A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050088



Internal ID21959321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36841623..36849208hg38UCSC Ensembl
chr20:35470026..35477611hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg387586
hg197586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636338
Samples
Known GenesSOGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050088
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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