A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498138



Internal ID22556073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72920778..72922427hg38UCSC Ensembl
chr5:72216605..72218254hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498138
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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