A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15260055



Internal ID5261871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58108701..58121492hg38UCSC Ensembl
Innerchr15:58108751..58121442hg38UCSC Ensembl
Outerchr15:58108651..58121542hg38UCSC Ensembl
chr15:58400900..58413691hg19UCSC Ensembl
Innerchr15:58400950..58413641hg19UCSC Ensembl
Outerchr15:58400850..58413741hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3812792
hg1912792
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636624
Supporting Variants
SamplesHG02784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15260055
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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