A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7342n100



Internal ID22793429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:145021961..145072757hg38UCSC Ensembl
chr8:146247347..146298143hg19UCSC Ensembl
chr8:146218151..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3850797
hg1950797
hg1850797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028370, nsv1017154, nsv1023359
Samples
Known GenesC8orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7342n100
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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