A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528748



Internal ID15109355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4780950..4971362hg38UCSC Ensembl
Innerchr7:4820581..5010993hg19UCSC Ensembl
Innerchr7:4787107..4977519hg18UCSC Ensembl
Innerchr7:4593822..4784234hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38190413
hg19190413
hg18190413
hg17190413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705409
Samples
Known GenesAP5Z1, MIR4656, MMD2, PAPOLB, RADIL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528748
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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