A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017847



Internal ID15965117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183098801..183099974hg38UCSC Ensembl
Innerchr4:184019954..184021127hg19UCSC Ensembl
Innerchr4:184256948..184258121hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381174
hg191174
hg181174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596341
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)nssv1017847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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