A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375358



Internal ID22601027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72319511..72324302hg38UCSC Ensembl
chr13:72893649..72898440hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg384792
hg194792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375358
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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