A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496637



Internal ID22554571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35999993..36002338hg38UCSC Ensembl
chr5:36000095..36002440hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843030
Supporting Variants
Samples
Known GenesUGT3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496637
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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