A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699227



Internal ID15435879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18896144..18899577hg38UCSC Ensembl
Innerchr7:18935767..18939200hg19UCSC Ensembl
Innerchr7:18902292..18905725hg18UCSC Ensembl
Innerchr7:18709007..18712440hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg383434
hg193434
hg183434
hg173434
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523468
Supporting Variants
Samples
Known GenesHDAC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699227
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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