A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1093604



Internal ID15946790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124970292..125033968hg38UCSC Ensembl
Innerchr7:124610346..124674022hg19UCSC Ensembl
Innerchr7:124397582..124461258hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3863677
hg1963677
hg1863677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608343
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)nssv1093604
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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