A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380979



Internal ID22438849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90702303..90703221hg38UCSC Ensembl
chr13:91354557..91355475hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380979
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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