A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013365



Internal ID18755896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20832431..21607455hg38UCSC Ensembl
Innerchr4:20834054..21609078hg19UCSC Ensembl
Innerchr4:20443152..21218176hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38775025
hg19775025
hg18775025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619888
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)nsv1013365
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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