A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6067n54



Internal ID22773962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73055458..73059104hg38UCSC Ensembl
chr18:70722693..70726339hg19UCSC Ensembl
chr18:68873673..68877319hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg383647
hg193647
hg183647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577628, nsv577627, nsv577634, nsv577630, nsv577633, nsv577635, nsv577629
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6067n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer