A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323957



Internal ID20857080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161626101..161628600hg38UCSC Ensembl
chr1:161595891..161598390hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201290
Samples
Known GenesFCGR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323957
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