A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7013n100



Internal ID22793100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11085419..11188885hg38UCSC Ensembl
chr8:10942929..11046394hg19UCSC Ensembl
chr8:10980339..11083804hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38103467
hg19103466
hg18103466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026331, nsv1025426
Samples
Known GenesXKR6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7013n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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