A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636633



Internal ID7023427
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15260122, essv15260123
SamplesHG01432, HG01125
Known GenesFAM63B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636633
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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