A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333142



Internal ID20866318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181202077..181234539hg38UCSC Ensembl
chr1:181171213..181203675hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3832463
hg1932463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333142
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