A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705277



Internal ID15441929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9806084..9835428hg38UCSC Ensembl
Innerchr2:9946213..9975557hg19UCSC Ensembl
Innerchr2:9863664..9893008hg18UCSC Ensembl
Innerchr2:9896811..9926155hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3829345
hg1929345
hg1829345
hg1729345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528645
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705277
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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