A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462977



Internal ID22520862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90556381..90557480hg38UCSC Ensembl
chr13:91208635..91209734hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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