A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7653n100



Internal ID22793740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63968448..64683570hg38UCSC Ensembl
chr9:69166365..69695988hg19UCSC Ensembl
chr9:68456185..68985808hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38715123
hg19529624
hg18529624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020401, nsv1030357, nsv1019181, nsv1022158
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)dgv7653n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer