A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495084



Internal ID22553017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18537151..18541896hg38UCSC Ensembl
chr5:18537260..18542005hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg384746
hg194746
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842527
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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