A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635619



Internal ID18587214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185450051..185594299hg38UCSC Ensembl
Innerchr4:186371205..186515453hg19UCSC Ensembl
Innerchr4:186608199..186752447hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38144249
hg19144249
hg18144249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029230
Supporting Variants
Samples
Known GenesCCDC110, PDLIM3, SORBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635619
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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