A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15260120



Internal ID1574248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58796663..58798249hg38UCSC Ensembl
Innerchr15:58796696..58798217hg38UCSC Ensembl
Outerchr15:58796631..58798282hg38UCSC Ensembl
chr15:59088862..59090448hg19UCSC Ensembl
Innerchr15:59088895..59090416hg19UCSC Ensembl
Outerchr15:59088830..59090481hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381587
hg191587
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636632
Supporting Variants
SamplesHG01459
Known GenesFAM63B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15260120
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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