A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962379



Internal ID15909649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:38000691..38065526hg38UCSC Ensembl
Innerchr3:38042182..38107017hg19UCSC Ensembl
Innerchr3:38017186..38082021hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3864836
hg1964836
hg1864836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590101
Supporting Variants
Samples
Known GenesDLEC1, PLCD1, VILL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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