A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590103



Internal ID16030826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39146691..39184636hg38UCSC Ensembl
Innerchr3:39188182..39226127hg19UCSC Ensembl
Innerchr3:39163186..39201131hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3837946
hg1937946
hg1837946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8287n54
Supporting Variantsnssv962381
Samples
Known GenesCSRNP1, XIRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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