A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419087



Internal ID22476957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57325185..57325295hg38UCSC Ensembl
chr5:56621012..56621122hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419087
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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