A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402455



Internal ID21060008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3331352..3336080hg38UCSC Ensembl
chr6:3331586..3336314hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384729
hg194729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142833
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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