A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454609



Internal ID22512485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109820723..109823722hg38UCSC Ensembl
chr13:110473070..110476069hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454609
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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