A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401059



Internal ID21058612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17412598..17880550hg38UCSC Ensembl
chr6:17412829..17880781hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38467953
hg19467953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6073n223
Supporting Variantsnssv18216155
Samples
Known GenesCAP2, FAM8A1, KIF13A, NUP153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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