A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496561



Internal ID20869764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19709901..19715800hg38UCSC Ensembl
chr16:19721223..19727122hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028165
Samples
Known GenesKNOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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