A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141971



Internal ID341171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77975775..77976588hg38UCSC Ensembl
chr9:80590691..80591504hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026000
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141971
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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