A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454795



Internal ID22512672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98364475..98441693hg38UCSC Ensembl
chr13:99016729..99093947hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3877219
hg1977219
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866214
Supporting Variants
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454795
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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