A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7518n100



Internal ID22793605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33728487..33798190hg38UCSC Ensembl
chr9:33728485..33798188hg19UCSC Ensembl
chr9:33718485..33788188hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3869704
hg1969704
hg1869704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019443, nsv1035024
Samples
Known GenesLOC101929688, PRSS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7518n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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