A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026917



Internal ID85667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101195305..101196212hg38UCSC Ensembl
chr9:103957587..103958494hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490204
Supporting Variants
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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