A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508937



Internal ID20882242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83843219..83939299hg38UCSC Ensembl
chr16:83876824..83972904hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3896081
hg1996081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190942
Samples
Known GenesMLYCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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