A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601169



Internal ID21793216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3567656..3567730hg38UCSC Ensembl
chr16:3617657..3617731hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032588
Supporting Variants
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601169
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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