A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937560



Internal ID22712930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104576182..104576831hg38UCSC Ensembl
chr13:105228533..105229182hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937560
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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