A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508168



Internal ID20881467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3418478..3445377hg38UCSC Ensembl
chr16:3468478..3495377hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3826900
hg1926900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029568
Samples
Known GenesNAA60, ZNF597
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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