A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592706



Internal ID16380115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186477534..186511434hg38UCSC Ensembl
Innerchr3:186195323..186229223hg19UCSC Ensembl
Innerchr3:187678017..187711917hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3833901
hg1933901
hg1833901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152561
Samples1780854205_A
Known GenesLOC253573
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592706
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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