A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4782n54



Internal ID22772677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100879147..100879954hg38UCSC Ensembl
chr15:101419352..101420159hg19UCSC Ensembl
chr15:99236875..99237682hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38808
hg19808
hg18808
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570808, nsv570807
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4782n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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