A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045644



Internal ID21954908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59928991..59929060hg38UCSC Ensembl
chr20:58504046..58504115hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631711
Samples
Known GenesSYCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045644
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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