A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279454



Internal ID5281271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68387073..68398737hg38UCSC Ensembl
Innerchr15:68387073..68398737hg38UCSC Ensembl
Outerchr15:68386573..68399237hg38UCSC Ensembl
chr15:68679412..68691076hg19UCSC Ensembl
Innerchr15:68679412..68691076hg19UCSC Ensembl
Outerchr15:68678912..68691576hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811665
hg1911665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636804
Supporting Variants
SamplesHG03779
Known GenesITGA11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279454
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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