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nsv930464

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 875 SVs from 64 studies. See in: genome view    
Remapped(Score: Pass):106,719,682-106,719,695Question Mark
Overlapping variant regions from other studies: 74 SVs from 19 studies. See in: genome view    
Remapped(Score: Pass):1,257,853-1,257,866Question Mark
Overlapping variant regions from other studies: 1635 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):1,211,360-1,211,374Question Mark
Overlapping variant regions from other studies: 892 SVs from 63 studies. See in: genome view    
Submitted genomic107,174,927-107,174,941Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartOuter Stop
nsv930464RemappedPassGRCh38.p12Primary AssemblySecond PassNC_000014.9Chr14-106,719,682106,719,695
nsv930464RemappedPassGRCh38.p12ALT_REF_LOCI_1Second PassNT_187600.1Chr14|NT_1
87600.1
-1,257,8531,257,866
nsv930464RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187600.1Chr14|NT_1
87600.1
1,211,360-1,211,374
nsv930464Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr14107,174,927-107,174,941

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1607661insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartOuter Stop
nssv1607661RemappedPerfectNT_187600.1:g.(?_1
257853)_(?_1257866
)ins38000NT_187600
.1:g.(1211360_?)_(
?_1211374)ins38000
GRCh38.p12Second PassNT_187600.1Chr14|NT_1
87600.1
1,211,360-1,211,374
nssv1607661RemappedPassNT_187600.1:g.(?_1
257853)_(?_1257866
)ins38000NT_187600
.1:g.(1211360_?)_(
?_1211374)ins38000
GRCh38.p12Second PassNT_187600.1Chr14|NT_1
87600.1
-1,257,8531,257,866
nssv1607661RemappedPassNC_000014.9:g.(?_1
06719682)_(?_10671
9695)ins38000
GRCh38.p12Second PassNC_000014.9Chr14-106,719,682106,719,695
nssv1607661Submitted genomicNC_000014.8:g.(107
174927_?)_(?_10717
4941)ins38000
GRCh37 (hg19)NC_000014.8Chr14107,174,927-107,174,941

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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