A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373057



Internal ID22598726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87291687..87311567hg38UCSC Ensembl
chr13:87943942..87963822hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3819881
hg1919881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373057
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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