A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486491



Internal ID22544406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158766012..158792344hg38UCSC Ensembl
chr3:158483801..158510133hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3826333
hg1926333
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835015
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486491
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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