A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032952



Internal ID20599992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84149916..84150239hg38UCSC Ensembl
chr16:84183521..84183844hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512197
Supporting Variants
Samples
Known GenesDNAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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