A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971555



Internal ID16265511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113947759..113948339hg38UCSC Ensembl
Innerchr3:113666606..113667186hg19UCSC Ensembl
Innerchr3:115149296..115149876hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38581
hg19581
hg18581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591318
Supporting Variants
Samples
Known GenesZDHHC23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971555
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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