A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3603n100



Internal ID20155219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43304322..43590925hg38UCSC Ensembl
chr19:43808474..44095077hg19UCSC Ensembl
chr19:48500314..48786917hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38286604
hg19286604
hg18286604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056721, nsv1058162
Samples
Known GenesCD177, ETHE1, IRGQ, LYPD3, PHLDB3, PINLYP, PRG1, TEX101, XRCC1, ZNF575
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3603n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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