A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484444



Internal ID22542353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126975619..126981068hg38UCSC Ensembl
chr3:126694462..126699911hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385450
hg195450
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484444
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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