A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023565



Internal ID21932908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84353738..84526127hg38UCSC Ensembl
chr16:84387344..84559733hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38172390
hg19172390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617878
Samples
Known GenesATP2C2, TLDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023565
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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