A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15355399



Internal ID1122292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:798001..812299hg38UCSC Ensembl
chr16:848001..862299hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814299
hg1914299
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637584
Supporting Variants
SamplesHG00759
Known GenesCHTF18, GNG13, PRR25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15355399
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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