A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063881



Internal ID18806412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4993052..5046059hg38UCSC Ensembl
Innerchr19:4993063..5046070hg19UCSC Ensembl
Innerchr19:4944063..4997070hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3853008
hg1953008
hg1853008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564608
Samples
Known GenesKDM4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063881
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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