A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636562



Internal ID7023356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55381779..55404610hg38UCSC Ensembl
Innerchr15:55381779..55404610hg38UCSC Ensembl
Outerchr15:55381279..55405110hg38UCSC Ensembl
chr15:55673977..55696808hg19UCSC Ensembl
Innerchr15:55673977..55696808hg19UCSC Ensembl
Outerchr15:55673477..55697308hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3822832
hg1922832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15256288
SamplesNA12413
Known GenesCCPG1, DYX1C1-CCPG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636562
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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