A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529001



Internal ID15109608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87911933..87934962hg38UCSC Ensembl
Innerchr7:87541248..87564277hg19UCSC Ensembl
Innerchr7:87379184..87402213hg18UCSC Ensembl
Innerchr7:87185899..87208928hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3823030
hg1923030
hg1823030
hg1723030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705707
Samples
Known GenesADAM22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529001
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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