A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7504n54



Internal ID22775399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15757441..15792231hg38UCSC Ensembl
chr20:15738086..15772876hg19UCSC Ensembl
chr20:15686086..15720876hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3834791
hg1934791
hg1834791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585641, nsv585642
Samples1780862459_A
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7504n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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