A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592120



Internal ID16379529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156908302..156973815hg38UCSC Ensembl
Innerchr3:156626091..156691604hg19UCSC Ensembl
Innerchr3:158108785..158174298hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3865514
hg1965514
hg1865514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv977129
Samples
Known GenesLEKR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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