A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380626



Internal ID22438496
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 StatusS
Merged Variantsnsv5931130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380626
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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