A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591191



Internal ID16378600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102748207..103368810hg38UCSC Ensembl
Innerchr3:102467051..103087654hg19UCSC Ensembl
Innerchr3:103949741..104570344hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38620604
hg19620604
hg18620604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152506
SamplesHGDP01095
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591191
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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