A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155353



Internal ID15507018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87203287..87911933hg38UCSC Ensembl
Innerchr7:86832603..87541248hg19UCSC Ensembl
Innerchr7:86670539..87379184hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38708647
hg19708646
hg18708646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607725
Supporting Variants
Samples1780854357_A
Known GenesABCB1, ABCB4, CROT, DBF4, RUNDC3B, SLC25A40, TMEM243, TP53TG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155353
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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