A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15535863



Internal ID5537679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80954497..81003876hg38UCSC Ensembl
chr16:80988394..81037481hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3849380
hg1949088
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639303
Supporting Variants
SamplesNA06985
Known GenesCMC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15535863
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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