A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017846



Internal ID16311802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183098699..183100083hg38UCSC Ensembl
Innerchr4:184019852..184021236hg19UCSC Ensembl
Innerchr4:184256846..184258230hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381385
hg191385
hg181385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596340
Supporting Variants
Samples
Known GenesWWC2, WWC2-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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