A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6157n54



Internal ID22774052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:404439..411003hg38UCSC Ensembl
chr19:404439..411003hg19UCSC Ensembl
chr19:355439..362003hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386565
hg196565
hg186565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578087, nsv578086
Samples
Known GenesC2CD4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6157n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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