A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931130



Internal ID22706409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32000186..32000575hg38UCSC Ensembl
chr13:32574323..32574712hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931130
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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