A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943422



Internal ID22718871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97546283..97546585hg38UCSC Ensembl
chr13:98198537..98198839hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943422
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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