A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591425



Internal ID16378834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123448885..123449789hg38UCSC Ensembl
Innerchr3:123167732..123168636hg19UCSC Ensembl
Innerchr3:124650422..124651326hg18UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38905
hg19905
hg18905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8532n54
Supporting Variantsnssv971805
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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