A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2261n100



Internal ID22788348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20359322..20422227hg38UCSC Ensembl
chr15:20564575..20627480hg19UCSC Ensembl
chr15:18824589..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3862906
hg1962906
hg1862906
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044397, nsv1050811
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2261n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss7
Observed Complex0
Frequencyn/a


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