A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497263



Internal ID20870469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50646734..50647524hg38UCSC Ensembl
chr16:50680645..50681435hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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