A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15398507



Internal ID1486668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19131300..19167136hg38UCSC Ensembl
chr16:19142622..19178458hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3835837
hg1935837
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638121
Supporting Variants
SamplesHG01366
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15398507
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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