A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2235n100



Internal ID22788322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20305889..20530173hg38UCSC Ensembl
chr15:20511142..20735411hg19UCSC Ensembl
chr15:18771156..18995425hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38224285
hg19224270
hg18224270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049169, nsv1045374, nsv1048639, nsv1053630, nsv1035994
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)dgv2235n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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