A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329135



Internal ID20862286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214884167..214885090hg38UCSC Ensembl
chr1:215057510..215058433hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329135
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