A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496954



Internal ID22554888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159229412..159242164hg38UCSC Ensembl
chr5:158656420..158669172hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3812753
hg1912753
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496954
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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