A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498774



Internal ID22556709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81341040..81342089hg38UCSC Ensembl
chr5:80636859..80637908hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842890
Supporting Variants
Samples
Known GenesACOT12, RNU5D-1, RNU5E-1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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