A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497614



Internal ID20870822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2969582..2975415hg38UCSC Ensembl
chr16:3019583..3025416hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385834
hg195834
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194254
Samples
Known GenesPAQR4, PKMYT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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