A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477220



Internal ID21134773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107655087..107660418hg38UCSC Ensembl
chr13:108307435..108312766hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385332
hg195332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007213
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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