A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591840



Internal ID16379249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302210..136308798hg38UCSC Ensembl
Innerchr3:136021052..136027640hg19UCSC Ensembl
Innerchr3:137503742..137510330hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg386589
hg196589
hg186589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974754
Samples
Known GenesPCCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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