A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147455



Internal ID346636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83049534..83055592hg38UCSC Ensembl
chr9:85664449..85670507hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386059
hg196059
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025353
Samples
Known GenesRASEF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147455
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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