A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147121



Internal ID346314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101102097..101108176hg38UCSC Ensembl
chr9:103864379..103870458hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg386080
hg196080
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025061
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147121
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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