A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15293111



Internal ID2055873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75758921..75763307hg38UCSC Ensembl
Innerchr15:75759421..75762807hg38UCSC Ensembl
Outerchr15:75757921..75764307hg38UCSC Ensembl
chr15:76051262..76055648hg19UCSC Ensembl
Innerchr15:76051762..76055148hg19UCSC Ensembl
Outerchr15:76050262..76056648hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384387
hg194387
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636929
Supporting Variants
SamplesHG01874
Known GenesMIR4313
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15293111
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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