A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497187



Internal ID20870392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84336197..84551801hg38UCSC Ensembl
chr16:84369803..84585407hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38215605
hg19215605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2953n223
Supporting Variantsnssv18032986
Samples
Known GenesATP2C2, TLDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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