A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6065n54



Internal ID22773960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71768203..71772119hg38UCSC Ensembl
chr18:69435439..69439355hg19UCSC Ensembl
chr18:67586419..67590335hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg383917
hg193917
hg183917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577605, nsv577606
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6065n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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