A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591193



Internal ID16378602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103163097..103232017hg38UCSC Ensembl
Innerchr3:102881941..102950861hg19UCSC Ensembl
Innerchr3:104364631..104433551hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3868921
hg1968921
hg1868921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv970922
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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