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nsv6147230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,418

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
Submitted genomic35,699,146-35,707,563Question Mark
Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):35,720,694-35,729,111Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1135,699,14635,707,563
nsv6147230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1135,720,69435,729,111

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17044247mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17044247Submitted genomicNC_000011.10:g.356
99146_35707563del
GRCh38 (hg38)NC_000011.10Chr1135,699,14635,707,563
nssv17044247RemappedPerfectNC_000011.9:g.3572
0694_35729111del
GRCh37.p13First PassNC_000011.9Chr1135,720,69435,729,111

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)
nssv170442470.0613926404
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