A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3648n100



Internal ID22789735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53420667..53522664hg38UCSC Ensembl
chr19:53923920..54025918hg19UCSC Ensembl
chr19:58615732..58717730hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38101998
hg19101999
hg18101999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060386, nsv1059161, nsv1063949, nsv1059427, nsv1066894, nsv1067398, nsv1065911, nsv1064511, nsv1065742, nsv1060334
Samples
Known GenesTPM3P9, ZNF331, ZNF761, ZNF813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3648n100
Frequency
Sample Size11257
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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