A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511851



Internal ID20885181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2913383..2938488hg38UCSC Ensembl
chr16:2963384..2988489hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3825106
hg1925106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184714
Samples
Known GenesFLYWCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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