A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079649



Internal ID15932835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18712375..18747940hg38UCSC Ensembl
Innerchr7:18751998..18787563hg19UCSC Ensembl
Innerchr7:18718523..18754088hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3835566
hg1935566
hg1835566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606359
Supporting Variants
Samples
Known GenesHDAC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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