A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635611



Internal ID18933892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184267146..184307462hg38UCSC Ensembl
Innerchr4:185188299..185228615hg19UCSC Ensembl
Innerchr4:185425293..185465609hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3840317
hg1940317
hg1840317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022143
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635611
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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