A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023794



Internal ID83576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81644735..81645101hg38UCSC Ensembl
chr9:84259650..84260016hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490051
Supporting Variants
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023794
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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