A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15489359



Internal ID2719609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58859813..58884152hg38UCSC Ensembl
Innerchr16:58859841..58884124hg38UCSC Ensembl
Outerchr16:58859785..58884180hg38UCSC Ensembl
chr16:58893717..58918056hg19UCSC Ensembl
Innerchr16:58893745..58918028hg19UCSC Ensembl
Outerchr16:58893689..58918084hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3824340
hg1924340
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638732
Supporting Variants
SamplesHG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15489359
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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