A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029770



Internal ID20596810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57046101..57048200hg38UCSC Ensembl
chr16:57080013..57082112hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498928
Supporting Variants
Samples
Known GenesNLRC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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