A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2650n100



Internal ID22788737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85745502..85801191hg38UCSC Ensembl
chr15:86288733..86344422hg19UCSC Ensembl
chr15:84089737..84145426hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3855690
hg1955690
hg1855690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051867, nsv1036705
Samples
Known GenesAKAP13, KLHL25, MIR1276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2650n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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