A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056391



Internal ID20623432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197169748..197171544hg38UCSC Ensembl
chr1:197138878..197140674hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg381797
hg191797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325369
Supporting Variants
Samples
Known GenesZBTB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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