A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15295754



Internal ID4558401
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636937
Supporting Variants
SamplesHG04060
Known GenesC15orf27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15295754
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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