A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7339n100



Internal ID20158955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144953363..145072757hg38UCSC Ensembl
chr8:146178749..146298143hg19UCSC Ensembl
chr8:146149553..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38119395
hg19119395
hg18119395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030844, nsv1029382, nsv1025660, nsv1024960, nsv1021855, nsv1021418
Samples
Known GenesC8orf33, TMED10P1, ZNF252P, ZNF252P-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7339n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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