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nsv6301785

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):26,672,000-26,680,000Question Mark
Overlapping variant regions from other studies: 141 SVs from 48 studies. See in: genome view    
Submitted genomic26,672,228-26,680,228Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6301785RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr626,672,00026,680,000
nsv6301785Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr626,672,22826,680,228

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17671798duplicationCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17671798RemappedPerfectNC_000006.12:g.266
72000_26680000dup		GRCh38.p12First PassNC_000006.12Chr626,672,00026,680,000
nssv17671798Submitted genomicNC_000006.11:g.266
72228_26680228dup		GRCh37 (hg19)NC_000006.11Chr626,672,22826,680,228

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)
nssv176717980.1318406404
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