A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499459



Internal ID22557394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8632057..8633457hg38UCSC Ensembl
chr5:8632169..8633569hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499459
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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