A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624857



Internal ID21816904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65477486..65478474hg38UCSC Ensembl
chr16:65511389..65512377hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027818
Supporting Variants
Samples
Known GenesLINC00922
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624857
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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