A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450999



Internal ID22508872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77457044..77468792hg38UCSC Ensembl
chr13:78031179..78042927hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3811749
hg1911749
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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