A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496851



Internal ID4698021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62808363..62816138hg38UCSC Ensembl
Innerchr16:62808863..62815638hg38UCSC Ensembl
Outerchr16:62807363..62817138hg38UCSC Ensembl
chr16:62842267..62850042hg19UCSC Ensembl
Innerchr16:62842767..62849542hg19UCSC Ensembl
Outerchr16:62841267..62851042hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387776
hg197776
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638803
Supporting Variants
SamplesHG04216
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496851
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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