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nsv6147073

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,756

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
Submitted genomic32,912,127-32,919,882Question Mark
Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):33,201,055-33,208,810Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147073Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1032,912,12732,919,882
nsv6147073RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1033,201,05533,208,810

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17032971mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17032971Submitted genomicNC_000010.11:g.329
12127_32919882del
GRCh38 (hg38)NC_000010.11Chr1032,912,12732,919,882
nssv17032971RemappedPerfectNC_000010.10:g.332
01055_33208810del
GRCh37.p13First PassNC_000010.10Chr1033,201,05533,208,810

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)
nssv17032971<0.00116404
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