A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971544



Internal ID16265500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113947504..113948442hg38UCSC Ensembl
Innerchr3:113666351..113667289hg19UCSC Ensembl
Innerchr3:115149041..115149979hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38939
hg19939
hg18939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591312
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)nssv971544
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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