A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7660n100



Internal ID22793747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64617909..64945771hg38UCSC Ensembl
chr9:69630327..69958189hg19UCSC Ensembl
chr9:68920147..69248009hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38327863
hg19327863
hg18327863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016792, nsv1024538, nsv1022133, nsv1030830, nsv1034299, nsv1018703
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)dgv7660n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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