A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590362



Internal ID16031085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56560707..56627292hg38UCSC Ensembl
Innerchr3:56594735..56661320hg19UCSC Ensembl
Innerchr3:56569775..56636360hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3866586
hg1966586
hg1866586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151892
Samples1780854231_A
Known GenesCCDC66, FAM208A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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