A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591322



Internal ID16378731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113947810..113948493hg38UCSC Ensembl
Innerchr3:113666657..113667340hg19UCSC Ensembl
Innerchr3:115149347..115150030hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38684
hg19684
hg18684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971582, nssv971581
Samples
Known GenesZDHHC23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591322
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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