A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679390



Internal ID15416042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:20727315..21055235hg38UCSC Ensembl
InnerchrX:20745433..21073353hg19UCSC Ensembl
InnerchrX:20655354..20983274hg18UCSC Ensembl
InnerchrX:20505090..20833010hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38327921
hg19327921
hg18327921
hg17327921
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)nssv679390
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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