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nsv5490620

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:924,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 4883 SVs from 127 studies. See in: genome view    
Submitted genomic6,692,000-7,616,000Question Mark
Overlapping variant regions from other studies: 4884 SVs from 127 studies. See in: genome view    
Remapped(Score: Perfect):6,549,521-7,473,522Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5490620Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr86,692,0007,616,000
nsv5490620RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr86,549,5217,473,522

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17006695duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17006695Submitted genomicNC_000008.11:g.669
2000_7616000dup
GRCh38 (hg38)NC_000008.11Chr86,692,0007,616,000
nssv17006695RemappedPerfectNC_000008.10:g.654
9521_7473522dup
GRCh37.p13First PassNC_000008.10Chr86,549,5217,473,522

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)
nssv17006695<0.00126394
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