A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591457



Internal ID16378866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:124887302..124887513hg38UCSC Ensembl
Innerchr3:124606149..124606360hg19UCSC Ensembl
Innerchr3:126088839..126089050hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38212
hg19212
hg18212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971888
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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