A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15535505



Internal ID712822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80907155..80920773hg38UCSC Ensembl
Innerchr16:80907655..80920273hg38UCSC Ensembl
Outerchr16:80906155..80921773hg38UCSC Ensembl
chr16:80941052..80954670hg19UCSC Ensembl
Innerchr16:80941552..80954170hg19UCSC Ensembl
Outerchr16:80940052..80955670hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3813619
hg1913619
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639297
Supporting Variants
SamplesHG00335
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15535505
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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