A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494898



Internal ID22552830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131104184..131128954hg38UCSC Ensembl
chr5:130439877..130464647hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3824771
hg1924771
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494898
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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