A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636937



Internal ID7023731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76080396..76085402hg38UCSC Ensembl
Innerchr15:76080546..76085252hg38UCSC Ensembl
Outerchr15:76080246..76085552hg38UCSC Ensembl
chr15:76372737..76377743hg19UCSC Ensembl
Innerchr15:76372887..76377593hg19UCSC Ensembl
Outerchr15:76372587..76377893hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg385007
hg195007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15295754
SamplesHG04060
Known GenesC15orf27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636937
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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