A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472631



Internal ID22530523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10541482..10543014hg38UCSC Ensembl
chr19:10652158..10653690hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869644
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472631
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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