A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614485



Internal ID20987556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116547701..116577500hg38UCSC Ensembl
chr6:116868864..116898663hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3829800
hg1929800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214530
Samples
Known GenesFAM26D, RWDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614485
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