A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140656



Internal ID339849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158998014..158999213hg38UCSC Ensembl
chr6:159419046..159420245hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989551
Samples
Known GenesRSPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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