A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463227



Internal ID22521113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76721686..76726672hg38UCSC Ensembl
chr13:77295821..77300807hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg384987
hg194987
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463227
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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