A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464868



Internal ID22522756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97867841..97877765hg38UCSC Ensembl
chr13:98520095..98530019hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg389925
hg199925
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464868
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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