A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15293126



Internal ID5503564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75873702..75883672hg38UCSC Ensembl
Innerchr15:75873713..75883662hg38UCSC Ensembl
Outerchr15:75873692..75883683hg38UCSC Ensembl
chr15:76166043..76176013hg19UCSC Ensembl
Innerchr15:76166054..76176003hg19UCSC Ensembl
Outerchr15:76166033..76176024hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg389971
hg199971
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636931
Supporting Variants
SamplesNA18986
Known GenesUBE2Q2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15293126
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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