A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140897



Internal ID340091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102170000..102175200hg38UCSC Ensembl
chr6:102617875..102623075hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140897
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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