A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15535522



Internal ID5537338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80920298..80965721hg38UCSC Ensembl
Innerchr16:80920349..80965671hg38UCSC Ensembl
Outerchr16:80920248..80965772hg38UCSC Ensembl
chr16:80954195..80999618hg19UCSC Ensembl
Innerchr16:80954246..80999568hg19UCSC Ensembl
Outerchr16:80954145..80999669hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3845424
hg1945424
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639300
Supporting Variants
SamplesHG03455
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15535522
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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