A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7217n100



Internal ID22793304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:51959888..52004909hg38UCSC Ensembl
chr8:52872448..52917469hg19UCSC Ensembl
chr8:53035001..53080022hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3845022
hg1945022
hg1845022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020673, nsv1031672
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)dgv7217n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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