A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6202n54



Internal ID22774097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1566455..1567450hg38UCSC Ensembl
chr19:1566454..1567449hg19UCSC Ensembl
chr19:1517454..1518449hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38996
hg19996
hg18996
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578309, nsv578301, nsv578307
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6202n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss3
Observed Complex0
Frequencyn/a


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