A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499365



Internal ID22557300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107012460..107016654hg38UCSC Ensembl
chr5:106348161..106352355hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg384195
hg194195
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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