A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685831



Internal ID109497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18962819..19048890hg38UCSC Ensembl
chr13:19536959..19623030hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3886072
hg1986072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499726
Supporting Variants
Samples
Known GenesLINC00442
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685831
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001874


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