A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478726



Internal ID22536628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5548648..5552697hg38UCSC Ensembl
chr19:5548659..5552708hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868456
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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