A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679314



Internal ID15415966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:20727315..20949500hg38UCSC Ensembl
InnerchrX:20745433..20967618hg19UCSC Ensembl
InnerchrX:20655354..20877539hg18UCSC Ensembl
InnerchrX:20505090..20727275hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38222186
hg19222186
hg18222186
hg17222186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517746
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679314
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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