A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029901



Internal ID19119120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18166156..18348333hg38UCSC Ensembl
Innerchr7:18205779..18387956hg19UCSC Ensembl
Innerchr7:18172304..18354481hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38182178
hg19182178
hg18182178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643234
Samples
Known GenesHDAC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029901
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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