A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725372



Internal ID149038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51173028..51173088hg38UCSC Ensembl
chr19:51676285..51676345hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524747
Supporting Variants
Samples
Known GenesSIGLEC17P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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