A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6533n54



Internal ID22774428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53096365..53124524hg38UCSC Ensembl
chr19:53599618..53627777hg19UCSC Ensembl
chr19:58291430..58319589hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3828160
hg1928160
hg1828160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580072, nsv580075, nsv580076, nsv580070, nsv580069
Samples1798860292_A, HGDP00214
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6533n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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