A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4577n54



Internal ID22772472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65524573..65530196hg38UCSC Ensembl
chr15:65816911..65822534hg19UCSC Ensembl
chr15:63603964..63609587hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385624
hg195624
hg185624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569758, nsv569728, nsv569761, nsv569772, nsv569779, nsv569766, nsv569785
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4577n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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