A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035119



Internal ID15888305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75052914..75053542hg38UCSC Ensembl
Innerchr5:74348739..74349367hg19UCSC Ensembl
Innerchr5:74384495..74385123hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38629
hg19629
hg18629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598661
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)nssv1035119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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