U.S. flag

An official website of the United States government

nsv5417066

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 18 studies. See in: genome view    
Submitted genomic76,078,547-76,078,572Question Mark
Overlapping variant regions from other studies: 80 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):76,544,890-76,544,915Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417066Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1476,078,54776,078,572
nsv5417066RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1476,544,89076,544,915

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697947alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697947Submitted genomicNC_000014.9:g.7607
8547_76078572ins28
1
GRCh38 (hg38)NC_000014.9Chr1476,078,54776,078,572
nssv17697947RemappedPerfectNC_000014.8:g.7654
4890_76544915ins28
1
GRCh37.p13First PassNC_000014.8Chr1476,544,89076,544,915

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17697947<0.00146404
Support Center