A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496932



Internal ID22554866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157876617..157885963hg38UCSC Ensembl
chr5:157303625..157312971hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg389347
hg199347
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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