nsv469525

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:164,475

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 270 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):14,801,735-14,966,209Question Mark
Overlapping variant regions from other studies: 270 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):14,941,859-15,106,333Question Mark
Overlapping variant regions from other studies: 2 SVs from 2 studies. See in: genome view    
Submitted genomic14,963,598-15,128,072Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469525RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000002.12Chr214,801,73514,966,209
nsv469525RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000002.11Chr214,941,85915,106,333
nsv469525Submitted genomicNCBI34 (hg16)GPC_000000200.1Chr214,963,59815,128,072

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1675583copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nssv1675583RemappedPerfectNC_000002.12:g.(?_
14801735)_(1496620
9_?)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000002.12Chr214,801,73514,966,209
nssv1675583RemappedPerfectNC_000002.11:g.(?_
14941859)_(1510633
3_?)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000002.11Chr214,941,85915,106,333
nssv1675583Submitted genomicGPC_000000200.1:g.
(?_14963598)_(1512
8072_?)del
NCBI34 (hg16)GPC_000000200.1Chr214,963,59815,128,072

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

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