A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021092



Internal ID21930435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49119701..49124889hg38UCSC Ensembl
chr13:49693837..49699025hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385189
hg195189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608990
Samples
Known GenesFNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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