A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15315949



Internal ID5108863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86979611..86981002hg38UCSC Ensembl
Innerchr15:86979661..86980952hg38UCSC Ensembl
Outerchr15:86979545..86981068hg38UCSC Ensembl
chr15:87522842..87524233hg19UCSC Ensembl
Innerchr15:87522892..87524183hg19UCSC Ensembl
Outerchr15:87522776..87524299hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637146
Supporting Variants
SamplesNA18558
Known GenesAGBL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15315949
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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