A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013194



Internal ID19102412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2368614..2426736hg38UCSC Ensembl
Innerchr4:2370341..2428463hg19UCSC Ensembl
Innerchr4:2340139..2398261hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3858123
hg1958123
hg1858123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616109
Samples
Known GenesLOC402160, ZFYVE28
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013194
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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