A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525802



Internal ID15106409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68033883..68051911hg38UCSC Ensembl
Innerchr2:68261015..68279043hg19UCSC Ensembl
Innerchr2:68114519..68132547hg18UCSC Ensembl
Innerchr2:68172666..68190694hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3818029
hg1918029
hg1818029
hg1718029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701986
Samples
Known GenesC1D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525802
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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