A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636638



Internal ID7023432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59109966..59112994hg38UCSC Ensembl
Innerchr15:59109966..59112994hg38UCSC Ensembl
Outerchr15:59109729..59113245hg38UCSC Ensembl
chr15:59402165..59405193hg19UCSC Ensembl
Innerchr15:59402165..59405193hg19UCSC Ensembl
Outerchr15:59401928..59405444hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383029
hg193029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261095, essv15261094
SamplesNA19036, HG01566
Known GenesCCNB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636638
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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