A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2597n100



Internal ID22788684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52973606..53024313hg38UCSC Ensembl
chr15:53265803..53316510hg19UCSC Ensembl
chr15:51053095..51103802hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3850708
hg1950708
hg1850708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042778, nsv1052623, nsv1037269
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2597n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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