A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516893



Internal ID15444186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18561742..18574896hg38UCSC Ensembl
Innerchr7:18601365..18614519hg19UCSC Ensembl
Innerchr7:18567890..18581044hg18UCSC Ensembl
Innerchr7:18374605..18387759hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813155
hg1913155
hg1813155
hg1713155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679032, nssv654738
Samples
Known GenesHDAC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516893
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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