A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332478



Internal ID20865650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197168001..197172100hg38UCSC Ensembl
chr1:197137131..197141230hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056388
Samples
Known GenesZBTB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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