A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437731



Internal ID22495601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3441831..3446541hg38UCSC Ensembl
chr6:3442065..3446775hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384711
hg194711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896772
Supporting Variants
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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