A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694370



Internal ID118036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90874180..91050049hg38UCSC Ensembl
chr13:91526434..91702303hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38175870
hg19175870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513375
Supporting Variants
Samples
Known GenesLINC00410
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694370
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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