A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032783



Internal ID20599823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81005362..81010091hg38UCSC Ensembl
chr16:81038967..81043696hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384730
hg194730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515067
Supporting Variants
Samples
Known GenesCENPN, CMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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