A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938237



Internal ID22713615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97867571..97877882hg38UCSC Ensembl
chr13:98519825..98530136hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3810312
hg1910312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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