A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743426



Internal ID20519414
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 StatusM
Merged Variants
Supporting Variantsnssv16272132
Samples
Known GenesNKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743426
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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