A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460309



Internal ID22518195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62858076..62869225hg38UCSC Ensembl
chr11:62625548..62636697hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3811150
hg1911150
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860239
Supporting Variants
Samples
Known GenesSLC3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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