A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635618



Internal ID18587213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185450051..185583318hg38UCSC Ensembl
Innerchr4:186371205..186504472hg19UCSC Ensembl
Innerchr4:186608199..186741466hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38133268
hg19133268
hg18133268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031570
Supporting Variants
Samples
Known GenesCCDC110, PDLIM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635618
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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