A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15261095



Internal ID5603630
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636638
Supporting Variants
SamplesNA19036
Known GenesCCNB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15261095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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