A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705421



Internal ID15442073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18841886..18842580hg38UCSC Ensembl
Innerchr7:18881509..18882203hg19UCSC Ensembl
Innerchr7:18848034..18848728hg18UCSC Ensembl
Innerchr7:18654749..18655443hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38695
hg19695
hg18695
hg17695
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528759
Supporting Variants
Samples
Known GenesHDAC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705421
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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