A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079647



Internal ID15586147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17898868..18335622hg38UCSC Ensembl
Innerchr7:17938491..18375245hg19UCSC Ensembl
Innerchr7:17905016..18341770hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38436755
hg19436755
hg18436755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606357
Supporting Variants
Samples
Known GenesHDAC9, PRPS1L1, SNX13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079647
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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