A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035116



Internal ID15888302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75052914..75053440hg38UCSC Ensembl
Innerchr5:74348739..74349265hg19UCSC Ensembl
Innerchr5:74384495..74385021hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38527
hg19527
hg18527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598660
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)nssv1035116
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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