A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590304



Internal ID16377713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52483190..52495250hg38UCSC Ensembl
Innerchr3:52517206..52529266hg19UCSC Ensembl
Innerchr3:52492246..52504306hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3812061
hg1912061
hg1812061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963091
Samples
Known GenesNISCH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590304
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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