A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032805



Internal ID20599845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81103984..81112905hg38UCSC Ensembl
chr16:81137589..81146510hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg388922
hg198922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500059
Supporting Variants
Samples
Known GenesPKD1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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