A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483094



Internal ID22541001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100148994..100164603hg38UCSC Ensembl
chr3:99867838..99883447hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3815610
hg1915610
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834239
Supporting Variants
Samples
Known GenesCMSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483094
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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