A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932556



Internal ID22707856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39856576..39858448hg38UCSC Ensembl
chr13:40430713..40432585hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381873
hg191873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932556
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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