A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591324



Internal ID16378733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113947961..113948313hg38UCSC Ensembl
Innerchr3:113666808..113667160hg19UCSC Ensembl
Innerchr3:115149498..115149850hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38353
hg19353
hg18353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971605
Samples
Known GenesZDHHC23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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