A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687024



Internal ID110690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39038109..39038850hg38UCSC Ensembl
chr13:39612246..39612987hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513078
Supporting Variants
Samples
Known GenesNHLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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