U.S. flag

An official website of the United States government

nsv5013700

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:153,681

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 710 SVs from 88 studies. See in: genome view    
Submitted genomic41,277,005-41,430,685Question Mark
Overlapping variant regions from other studies: 708 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):39,433,257-39,586,937Question Mark
Overlapping variant regions from other studies: 92 SVs from 26 studies. See in: genome view    
Remapped(Score: Pass):16,589-119,548Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5013700Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,277,00541,430,685
nsv5013700RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,433,25739,586,937
nsv5013700RemappedPassGRCh37.p13PATCHESFirst PassNW_003315953.1Chr17|NW_0
03315953.1
16,589119,548

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16576122duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16576122Submitted genomicNC_000017.11:g.412
77005_41430685dup
GRCh38 (hg38)NC_000017.11Chr1741,277,00541,430,685
nssv16576122RemappedPassNW_003315953.1:g.1
6589_119548dup
GRCh37.p13First PassNW_003315953.1Chr17|NW_0
03315953.1
16,589119,548
nssv16576122RemappedPerfectNC_000017.10:g.394
33257_39586937dup
GRCh37.p13First PassNC_000017.10Chr1739,433,25739,586,937

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16576122<0.001129246
Support Center