A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15428357



Internal ID1975044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23762421..23766473hg38UCSC Ensembl
Innerchr16:23762457..23766437hg38UCSC Ensembl
Outerchr16:23762385..23766509hg38UCSC Ensembl
chr16:23773742..23777794hg19UCSC Ensembl
Innerchr16:23773778..23777758hg19UCSC Ensembl
Outerchr16:23773706..23777830hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384053
hg194053
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638237
Supporting Variants
SamplesHG01841
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15428357
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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