A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057373



Internal ID18799904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4963155..5037404hg38UCSC Ensembl
Innerchr19:4963166..5037415hg19UCSC Ensembl
Innerchr19:4914166..4988415hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3874250
hg1974250
hg1874250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723254
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)nsv1057373
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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