A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142416



Internal ID341616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109523565..109524319hg38UCSC Ensembl
chr9:112285845..112286599hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142416
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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