A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335585



Internal ID20868779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181120341..181145457hg38UCSC Ensembl
chr1:181089477..181114593hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3825117
hg1925117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335585
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