A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15260123



Internal ID1548795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58808740..58809916hg38UCSC Ensembl
Innerchr15:58808805..58809852hg38UCSC Ensembl
Outerchr15:58808676..58809981hg38UCSC Ensembl
chr15:59100939..59102115hg19UCSC Ensembl
Innerchr15:59101004..59102051hg19UCSC Ensembl
Outerchr15:59100875..59102180hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636633
Supporting Variants
SamplesHG01432
Known GenesFAM63B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15260123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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