A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378551



Internal ID22436421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94773768..94774388hg38UCSC Ensembl
chr13:95426022..95426642hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378551
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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