A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7658n100



Internal ID22793745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64462496..64965592hg38UCSC Ensembl
chr9:69474914..69978010hg19UCSC Ensembl
chr9:68764734..69267830hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38503097
hg19503097
hg18503097
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033836, nsv1026445
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7658n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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