A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142491



Internal ID341691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67677387..67684387hg38UCSC Ensembl
chr9:46343226..46350226hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142491
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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