A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6238n54



Internal ID22774133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6951556..7000390hg38UCSC Ensembl
chr19:6951567..7000401hg19UCSC Ensembl
chr19:6902567..6951401hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3848835
hg1948835
hg1848835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578473, nsv578478, nsv578474
SamplesHGDP01078, HGDP01147
Known GenesEMR4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6238n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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