A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696899



Internal ID15433551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35200463..35636817hg38UCSC Ensembl
Innerchr2:35425529..35861883hg19UCSC Ensembl
Innerchr2:35279033..35715387hg18UCSC Ensembl
Innerchr2:35337180..35773534hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38436355
hg19436355
hg18436355
hg17436355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519522
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696899
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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