A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028949



Internal ID15882135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35505580..35577155hg38UCSC Ensembl
Innerchr5:35505682..35577257hg19UCSC Ensembl
Innerchr5:35541439..35613014hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3871576
hg1971576
hg1871576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597812
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)nssv1028949
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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