A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6292n54



Internal ID22774187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17150557..17150908hg38UCSC Ensembl
chr19:17261367..17261718hg19UCSC Ensembl
chr19:17122367..17122718hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38352
hg19352
hg18352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578737, nsv578738
Samples
Known GenesMYO9B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6292n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss145
Observed Complex0
Frequencyn/a


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