A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6021n54



Internal ID22773916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68583998..68653928hg38UCSC Ensembl
chr18:66251235..66321165hg19UCSC Ensembl
chr18:64402215..64472145hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3869931
hg1969931
hg1869931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577368, nsv577367
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6021n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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