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  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:444,192

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2645 SVs from 103 studies. See in: genome view    
Remapped(Score: Good):22,620,066-23,064,257Question Mark
Overlapping variant regions from other studies: 2937 SVs from 108 studies. See in: genome view    
Submitted genomic22,808,811-23,253,030Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4678842RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1522,620,06623,064,257
nsv4678842Submitted genomicGRCh37.p13Primary AssemblyNC_000015.9Chr1522,808,81123,253,030

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16211774deletionSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
GRCh38.p12First PassNC_000015.10Chr1522,620,06623,064,257
nssv16211774Submitted genomicNC_000015.9:g.(?_2

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)
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