A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508751



Internal ID20882055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1915523..1948184hg38UCSC Ensembl
chr16:1965524..1998185hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3832662
hg1932662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186347
Samples
Known GenesHS3ST6, MSRB1, RPL3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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