A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7659n100



Internal ID22793746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64493516..64965592hg38UCSC Ensembl
chr9:69505934..69978010hg19UCSC Ensembl
chr9:68795754..69267830hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38472077
hg19472077
hg18472077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017460, nsv1026697, nsv1022125, nsv1030011, nsv1020573, nsv1034953, nsv1028310, nsv1034405
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)dgv7659n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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