A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15321852



Internal ID6844794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93321156..93327601hg38UCSC Ensembl
Innerchr15:93321156..93327601hg38UCSC Ensembl
Outerchr15:93320656..93328101hg38UCSC Ensembl
chr15:93864385..93870830hg19UCSC Ensembl
Innerchr15:93864385..93870830hg19UCSC Ensembl
Outerchr15:93863885..93871330hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386446
hg196446
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637287
Supporting Variants
SamplesNA20911
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15321852
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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