A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608346



Internal ID16395755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:125322031..125356733hg38UCSC Ensembl
Innerchr7:124962085..124996787hg19UCSC Ensembl
Innerchr7:124749321..124784023hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3834703
hg1934703
hg1834703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093606
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608346
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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