A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513997



Internal ID20887346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:739071..772337hg38UCSC Ensembl
chr16:789071..822337hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3833267
hg1933267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194578
Samples
Known GenesMIR662, MSLN, NARFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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