A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639131



Internal ID7025914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76596810..76620635hg38UCSC Ensembl
chr16:76630707..76654532hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3823826
hg1923826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15526591
SamplesNA20765
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639131
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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