A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6220n54



Internal ID22774115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2701508..2702293hg38UCSC Ensembl
chr19:2701506..2702291hg19UCSC Ensembl
chr19:2652506..2653291hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38786
hg19786
hg18786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578394, nsv578392, nsv578391, nsv578393
Samples
Known GenesGNG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6220n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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