A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2265n100



Internal ID22788352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20367351..20512131hg38UCSC Ensembl
chr15:20572604..20717374hg19UCSC Ensembl
chr15:18832618..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38144781
hg19144771
hg18144771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037006, nsv1050286, nsv1038645, nsv1047962, nsv1037390, nsv1044890, nsv1046679, nsv1047340
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)dgv2265n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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