A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592153



Internal ID16379562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162160925..162258943hg38UCSC Ensembl
Innerchr3:161878713..161976731hg19UCSC Ensembl
Innerchr3:163361407..163459425hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3898019
hg1998019
hg1898019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153396
SamplesNINDS_67
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592153
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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