A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3615n100



Internal ID19013983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48236633..48264769hg38UCSC Ensembl
chr19:48739890..48768026hg19UCSC Ensembl
chr19:53431702..53459838hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3828137
hg1928137
hg1828137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062566, nsv1063725
Samples
Known GenesCARD8, LOC100505812
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3615n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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