A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490204



Internal ID267464
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 StatusM
Merged Variants
Supporting Variantsnssv17026917
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490204
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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