A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10875n54



Internal ID22778770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102992625..103769899hg38UCSC Ensembl
chr6:103440500..104217774hg19UCSC Ensembl
chr6:103547193..104324467hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38777275
hg19777275
hg18777275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604337, nsv604333
SamplesHGDP00731, HGDP00683
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10875n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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