A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6022n54



Internal ID22773917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69006355..69067898hg38UCSC Ensembl
chr18:66673592..66735135hg19UCSC Ensembl
chr18:64824572..64886115hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3861544
hg1961544
hg1861544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577377, nsv577383
SamplesNINDS_223
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6022n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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