A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489602



Internal ID22547522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127826046..127828227hg38UCSC Ensembl
chr3:127544889..127547070hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382182
hg192182
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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