A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15260116



Internal ID3107678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58788984..58790902hg38UCSC Ensembl
Innerchr15:58789034..58790852hg38UCSC Ensembl
Outerchr15:58788912..58790974hg38UCSC Ensembl
chr15:59081183..59083101hg19UCSC Ensembl
Innerchr15:59081233..59083051hg19UCSC Ensembl
Outerchr15:59081111..59083173hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381919
hg191919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636631
Supporting Variants
SamplesHG02728
Known GenesFAM63B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15260116
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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