A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589285



Internal ID16030008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:211890..255638hg38UCSC Ensembl
Innerchr3:253573..297321hg19UCSC Ensembl
Innerchr3:228573..272321hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3843749
hg1943749
hg1843749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957798
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589285
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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