A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515135



Internal ID20888493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71240528..71283442hg38UCSC Ensembl
chr16:71274431..71317345hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3842915
hg1942915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180309
Samples
Known GenesCMTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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