A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676586



Internal ID15413238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14216802..14226725hg38UCSC Ensembl
Innerchr2:14356926..14366849hg19UCSC Ensembl
Innerchr2:14274377..14284300hg18UCSC Ensembl
Innerchr2:14307524..14317447hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg389924
hg199924
hg189924
hg179924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676586
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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