A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279455



Internal ID1567547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68458402..68464929hg38UCSC Ensembl
Innerchr15:68458402..68464929hg38UCSC Ensembl
Outerchr15:68458163..68465155hg38UCSC Ensembl
chr15:68750741..68757268hg19UCSC Ensembl
Innerchr15:68750741..68757268hg19UCSC Ensembl
Outerchr15:68750502..68757494hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386528
hg196528
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636805
Supporting Variants
SamplesHG01447
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279455
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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