A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592124



Internal ID16379533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158837189..158918268hg38UCSC Ensembl
Innerchr3:158554978..158636057hg19UCSC Ensembl
Innerchr3:160037672..160118751hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3881080
hg1981080
hg1881080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv977133
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592124
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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