A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2657n100



Internal ID22788744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90283720..90318370hg38UCSC Ensembl
chr15:90826952..90861602hg19UCSC Ensembl
chr15:88627956..88662606hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3834651
hg1934651
hg1834651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054724, nsv1037105
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)dgv2657n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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