A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15537875



Internal ID5539691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81755626..81815373hg38UCSC Ensembl
Innerchr16:81755626..81815373hg38UCSC Ensembl
Outerchr16:81755126..81815873hg38UCSC Ensembl
chr16:81789231..81848978hg19UCSC Ensembl
Innerchr16:81789231..81848978hg19UCSC Ensembl
Outerchr16:81788731..81849478hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3859748
hg1959748
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639343
Supporting Variants
SamplesHG02661
Known GenesPLCG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15537875
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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