A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473286



Internal ID22531179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16248210..16256362hg38UCSC Ensembl
chr19:16359021..16367173hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg388153
hg198153
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473286
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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