A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029645



Internal ID21938988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50563913..50563975hg38UCSC Ensembl
chr16:50597824..50597886hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623054
Samples
Known GenesNKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029645
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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