A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485211



Internal ID22543122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14415474..14420982hg38UCSC Ensembl
chr3:14456982..14462490hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg385509
hg195509
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835254
Supporting Variants
Samples
Known GenesSLC6A6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485211
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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