A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381864



Internal ID22439734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38511504..38512007hg38UCSC Ensembl
chr13:39085641..39086144hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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