A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656359



Internal ID15393011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240482563..240490632hg38UCSC Ensembl
Innerchr2:241421980..241430049hg19UCSC Ensembl
Innerchr2:241070653..241078722hg18UCSC Ensembl
Innerchr2:241141970..241150039hg17UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg388070
hg198070
hg188070
hg178070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515975
Supporting Variants
Samples
Known GenesANKMY1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656359
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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