A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15213291



Internal ID5215107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35238426..35243735hg38UCSC Ensembl
Innerchr15:35238926..35243235hg38UCSC Ensembl
Outerchr15:35237426..35244735hg38UCSC Ensembl
chr15:35530627..35535936hg19UCSC Ensembl
Innerchr15:35531127..35535436hg19UCSC Ensembl
Outerchr15:35529627..35536936hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385310
hg195310
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636132
Supporting Variants
SamplesHG00690
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15213291
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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