A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591836



Internal ID16379245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302210..136306294hg38UCSC Ensembl
Innerchr3:136021052..136025136hg19UCSC Ensembl
Innerchr3:137503742..137507826hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384085
hg194085
hg184085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8613n54
Supporting Variantsnssv974392, nssv974391, nssv974390
Samples
Known GenesPCCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591836
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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