A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493323



Internal ID22551252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57549494..57551319hg38UCSC Ensembl
chr3:57535221..57537046hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836385
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493323
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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