U.S. flag

An official website of the United States government

nsv1151475

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:89

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 497 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):189,835,682-189,835,770Question Mark
Overlapping variant regions from other studies: 66 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):484,411-484,499Question Mark
Overlapping variant regions from other studies: 52 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):169,208-169,296Question Mark
Overlapping variant regions from other studies: 58 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):169,208-169,296Question Mark
Overlapping variant regions from other studies: 498 SVs from 58 studies. See in: genome view    
Submitted genomic190,756,837-190,756,925Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv1151475RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4189,835,682189,835,770
nsv1151475RemappedPerfectGRCh38.p12ALT_REF_LOCI_3Second PassNT_187679.1Chr4|NT_18
7679.1
484,411484,499
nsv1151475RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187543.1Chr4|NT_18
7543.1
169,208169,296
nsv1151475RemappedPerfectGRCh38.p12ALT_REF_LOCI_2Second PassNT_187650.1Chr4|NT_18
7650.1
169,208169,296
nsv1151475Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4190,756,837190,756,925

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv4004040deletionKWB1SequencingRead depth and paired-end mapping8,440

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv4004040RemappedPerfectNT_187679.1:g.(484
411_?)_(?_484499)d
el
GRCh38.p12Second PassNT_187679.1Chr4|NT_18
7679.1
484,411484,499
nssv4004040RemappedPerfectNT_187543.1:g.(169
208_?)_(?_169296)d
el
GRCh38.p12Second PassNT_187543.1Chr4|NT_18
7543.1
169,208169,296
nssv4004040RemappedPerfectNT_187650.1:g.(169
208_?)_(?_169296)d
el
GRCh38.p12Second PassNT_187650.1Chr4|NT_18
7650.1
169,208169,296
nssv4004040RemappedPerfectNC_000004.12:g.(18
9835682_?)_(?_1898
35770)del
GRCh38.p12First PassNC_000004.12Chr4189,835,682189,835,770
nssv4004040Submitted genomicNC_000004.11:g.(19
0756837_?)_(?_1907
56925)del
GRCh37 (hg19)NC_000004.11Chr4190,756,837190,756,925

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center