A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15359757



Internal ID3939958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1356693..1364925hg38UCSC Ensembl
chr16:1406694..1414926hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388233
hg198233
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637616
Supporting Variants
SamplesHG03594
Known GenesGNPTG, UNKL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15359757
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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