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nsv6141047

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 366 SVs from 43 studies. See in: genome view    
Submitted genomic70,177,807-70,183,807Question Mark
Overlapping variant regions from other studies: 366 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):69,473,634-69,479,634Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6141047Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr570,177,80770,183,807
nsv6141047RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr569,473,63469,479,634

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967453deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967453Submitted genomicNC_000005.10:g.701
77807_70183807del
GRCh38 (hg38)NC_000005.10Chr570,177,80770,183,807
nssv16967453RemappedPerfectNC_000005.9:g.6947
3634_69479634del
GRCh37.p13First PassNC_000005.9Chr569,473,63469,479,634

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)
nssv169674530.67931004564
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