A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965599



Internal ID15912869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74105982..74172342hg38UCSC Ensembl
Innerchr3:74155133..74221493hg19UCSC Ensembl
Innerchr3:74237823..74304183hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3866361
hg1966361
hg1866361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590640
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv965599
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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