A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500268



Internal ID20873493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3342217..3344600hg38UCSC Ensembl
chr16:3392217..3394600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382384
hg192384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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