A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431853



Internal ID22489723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43197208..43197644hg38UCSC Ensembl
chr6:43164946..43165382hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906862
Supporting Variants
Samples
Known GenesCUL9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431853
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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