A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142565



Internal ID341766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60568600..60601000hg38UCSC Ensembl
chr9_gl000199_random:50042..82442hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3832401
hg1932401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142565
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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