A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7256n100



Internal ID22793343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85579538..85645172hg38UCSC Ensembl
chr8:86491767..86557401hg19UCSC Ensembl
chr8:86679019..86744653hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3865635
hg1965635
hg1865635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026966, nsv1017417, nsv1026714
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)dgv7256n100
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