A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141431



Internal ID340627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40691948..40886100hg38UCSC Ensembl
chr9:66664196..66839128hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38194153
hg19174933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141431
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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