A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017982



Internal ID15965252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185451672..185605031hg38UCSC Ensembl
Innerchr4:186372826..186526185hg19UCSC Ensembl
Innerchr4:186609820..186763179hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38153360
hg19153360
hg18153360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596373
Supporting Variants
Samples
Known GenesCCDC110, PDLIM3, SORBS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017982
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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