A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15399272



Internal ID4988827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19977128..19981213hg38UCSC Ensembl
chr16:19988450..19992535hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638129
Supporting Variants
SamplesNA18489
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15399272
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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