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nsv6147345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,354

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
Submitted genomic30,945,183-30,953,536Question Mark
Overlapping variant regions from other studies: 99 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):31,234,112-31,242,465Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1030,945,18330,953,536
nsv6147345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1031,234,11231,242,465

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17030476mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17030476Submitted genomicNC_000010.11:g.309
45183_30953536del
GRCh38 (hg38)NC_000010.11Chr1030,945,18330,953,536
nssv17030476RemappedPerfectNC_000010.10:g.312
34112_31242465del
GRCh37.p13First PassNC_000010.10Chr1031,234,11231,242,465

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)
nssv17030476<0.00116404
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