A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020263



Internal ID21929606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86505609..86505662hg38UCSC Ensembl
chr10:88265366..88265419hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594917
Samples
Known GenesWAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020263
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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