A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591648



Internal ID16379057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128712098..128715577hg38UCSC Ensembl
Innerchr3:128430941..128434420hg19UCSC Ensembl
Innerchr3:129913631..129917110hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg383480
hg193480
hg183480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973097
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591648
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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