A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272132



Internal ID20481350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50579398..50579515hg38UCSC Ensembl
chr16:50613309..50613426hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743426
Supporting Variants
Samples
Known GenesNKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272132
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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