A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049268



Internal ID21958501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56527056..56536111hg38UCSC Ensembl
chr20:55102112..55111167hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg389056
hg199056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636788
Samples
Known GenesFAM209B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049268
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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