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nsv6308647

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,904

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):29,992,070-29,999,973Question Mark
Overlapping variant regions from other studies: 80 SVs from 25 studies. See in: genome view    
Submitted genomic30,033,561-30,041,464Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6308647RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr329,992,07029,999,973
nsv6308647Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr330,033,56130,041,464

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17661319mobile element deletionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17661319RemappedPerfectNC_000003.12:g.299
92070_29999973del
GRCh38.p12First PassNC_000003.12Chr329,992,07029,999,973
nssv17661319Submitted genomicNC_000003.11:g.300
33561_30041464del
GRCh37 (hg19)NC_000003.11Chr330,033,56130,041,464

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv176613190.013836404
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