A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468889



Internal ID22526779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40058673..40073360hg38UCSC Ensembl
chr13:40632810..40647497hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3814688
hg1914688
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468889
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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