A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6022n100



Internal ID22792109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76879502..77117701hg38UCSC Ensembl
chr6:77589219..77827418hg19UCSC Ensembl
chr6:77645938..77884137hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38238200
hg19238200
hg18238200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021812, nsv1026517
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6022n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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