A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410472



Internal ID21068025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54889229..54889542hg38UCSC Ensembl
chr6:54754027..54754340hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143513
Samples
Known GenesFAM83B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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