A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619891



Internal ID18918172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:21268735..21477404hg38UCSC Ensembl
Innerchr4:21270358..21479027hg19UCSC Ensembl
Innerchr4:20879456..21088125hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38208670
hg19208670
hg18208670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014062
Supporting Variants
Samples
Known GenesKCNIP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3619891
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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