A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524365



Internal ID15451658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3147886..3159967hg38UCSC Ensembl
Innerchr2:3151657..3163738hg19UCSC Ensembl
Innerchr2:3130664..3142745hg18UCSC Ensembl
Innerchr2:4689940..4702021hg17UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3812082
hg1912082
hg1812082
hg1712082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700276
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524365
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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