A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15326046



Internal ID5995471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95294970..95295850hg38UCSC Ensembl
Innerchr15:95294970..95295850hg38UCSC Ensembl
Outerchr15:95294574..95296245hg38UCSC Ensembl
chr15:95838199..95839079hg19UCSC Ensembl
Innerchr15:95838199..95839079hg19UCSC Ensembl
Outerchr15:95837803..95839474hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637330
Supporting Variants
SamplesNA19395
Known GenesLOC400456
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15326046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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