A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143700



Internal ID342901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88450..184000hg38UCSC Ensembl
chr11:88450..184000hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3895551
hg1995551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65n206
Supporting Variantsnssv17043540
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143700
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer