A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490330



Internal ID22548252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172611898..172622802hg38UCSC Ensembl
chr3:172329688..172340592hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810905
hg1910905
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490330
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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