A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083672



Internal ID15936858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47049540..47052335hg38UCSC Ensembl
Innerchr7:47089138..47091933hg19UCSC Ensembl
Innerchr7:47055663..47058458hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg382796
hg192796
hg182796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606851
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)nssv1083672
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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