A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7655n100



Internal ID22793742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64462496..64847603hg38UCSC Ensembl
chr9:69474914..69860021hg19UCSC Ensembl
chr9:68764734..69149841hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38385108
hg19385108
hg18385108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022085, nsv1033367, nsv1016756, nsv1024606, nsv1019825, nsv1032458, nsv1018264
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)dgv7655n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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