A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10657n54



Internal ID22778552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51330498..51336459hg38UCSC Ensembl
chr6:51195296..51201257hg19UCSC Ensembl
chr6:51303255..51309216hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg385962
hg195962
hg185962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603092, nsv603094, nsv603095, nsv603093
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10657n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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