A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376611



Internal ID22602280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40030343..40031233hg38UCSC Ensembl
chr13:40604480..40605370hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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