A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2656n100



Internal ID22788743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87353113..87370306hg38UCSC Ensembl
chr15:87896344..87913537hg19UCSC Ensembl
chr15:85697348..85714541hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3817194
hg1917194
hg1817194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044972, nsv1047161
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)dgv2656n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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