A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079190



Internal ID15932376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12867553..13037440hg38UCSC Ensembl
Innerchr7:12907178..13077065hg19UCSC Ensembl
Innerchr7:12873703..13043590hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38169888
hg19169888
hg18169888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606238
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079190
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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