A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15555120



Internal ID6644670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87218579..87289576hg38UCSC Ensembl
Innerchr16:87218579..87289576hg38UCSC Ensembl
Outerchr16:87218079..87290076hg38UCSC Ensembl
chr16:87252185..87323182hg19UCSC Ensembl
Innerchr16:87252185..87323182hg19UCSC Ensembl
Outerchr16:87251685..87323682hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3870998
hg1970998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639505
Supporting Variants
SamplesNA20800
Known GenesLOC101928682
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15555120
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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