A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508223



Internal ID20881522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28888052..28888284hg38UCSC Ensembl
chr16:28899373..28899605hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029058
Samples
Known GenesATP2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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