A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1081506



Internal ID15588006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26197313..26203488hg38UCSC Ensembl
Innerchr7:26236933..26243108hg19UCSC Ensembl
Innerchr7:26203458..26209633hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg386176
hg196176
hg186176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606459
Supporting Variants
Samples
Known GenesCBX3, HNRNPA2B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1081506
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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