A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7654n100



Internal ID22793741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63968448..64818927hg38UCSC Ensembl
chr9:69178874..69831345hg19UCSC Ensembl
chr9:68468694..69121165hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38850480
hg19652472
hg18652472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027536, nsv1023332
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6, LOC100133920, LOC440896
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7654n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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