A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364671



Internal ID22590340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106831756..106832578hg38UCSC Ensembl
chr13:107484104..107484926hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364671
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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