A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145864



Internal ID20712904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5592399..5630733hg38UCSC Ensembl
chr6:5592632..5630966hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3838335
hg1938335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413094
Supporting Variants
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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