A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15537876



Internal ID3025082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81818137..81867692hg38UCSC Ensembl
Innerchr16:81818137..81867692hg38UCSC Ensembl
Outerchr16:81817637..81868192hg38UCSC Ensembl
chr16:81851742..81901297hg19UCSC Ensembl
Innerchr16:81851742..81901297hg19UCSC Ensembl
Outerchr16:81851242..81901797hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3849556
hg1949556
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639344
Supporting Variants
SamplesHG02661
Known GenesPLCG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15537876
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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