A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140414



Internal ID339607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110772883..110773110hg38UCSC Ensembl
chr6:111094086..111094313hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987998
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140414
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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