A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502551



Internal ID20875797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28888290..28897634hg38UCSC Ensembl
chr16:28899611..28908955hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg389345
hg199345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029059
Samples
Known GenesATP2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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