A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059033



Internal ID20626073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233991201..233993000hg38UCSC Ensembl
chr1:234126947..234128746hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321467
Supporting Variants
Samples
Known GenesSLC35F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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