A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017844



Internal ID15965114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183098699..183099862hg38UCSC Ensembl
Innerchr4:184019852..184021015hg19UCSC Ensembl
Innerchr4:184256846..184258009hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381164
hg191164
hg181164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596339
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)nssv1017844
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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