A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523497



Internal ID15450790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18856388..18919758hg38UCSC Ensembl
Innerchr7:18896011..18959381hg19UCSC Ensembl
Innerchr7:18862536..18925906hg18UCSC Ensembl
Innerchr7:18669251..18732621hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3863371
hg1963371
hg1863371
hg1763371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699266
Samples
Known GenesHDAC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523497
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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