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nsv6147317

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,271

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 127 SVs from 34 studies. See in: genome view    
Submitted genomic67,577,572-67,586,842Question Mark
Overlapping variant regions from other studies: 127 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):69,337,330-69,346,600Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147317Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1067,577,57267,586,842
nsv6147317RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1069,337,33069,346,600

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037339mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037339Submitted genomicNC_000010.11:g.675
77572_67586842del
GRCh38 (hg38)NC_000010.11Chr1067,577,57267,586,842
nssv17037339RemappedPerfectNC_000010.10:g.693
37330_69346600del
GRCh37.p13First PassNC_000010.10Chr1069,337,33069,346,600

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)
nssv17037339<0.00126404
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