A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493250



Internal ID22551179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53308281..53319601hg38UCSC Ensembl
chr3:53342311..53353628hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3811321
hg1911318
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836373
Supporting Variants
Samples
Known GenesDCP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493250
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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