A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592705



Internal ID16380114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:185937136..185962797hg38UCSC Ensembl
Innerchr3:185654924..185680586hg19UCSC Ensembl
Innerchr3:187137618..187163280hg18UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3825662
hg1925663
hg1825663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152560
SamplesHGDP01300
Known GenesLOC344887, TRA2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592705
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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