A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029407



Internal ID20596447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3543384..3546296hg38UCSC Ensembl
chr16:3593384..3596296hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505618
Supporting Variants
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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