A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611285



Internal ID21803332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23583603..23583663hg38UCSC Ensembl
chr16:23594924..23594984hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022705
Supporting Variants
Samples
Known GenesNDUFAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611285
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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