A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479733



Internal ID22537635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85604624..85605919hg38UCSC Ensembl
chr16:85638230..85639525hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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