A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325540



Internal ID20858671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151926043..151927391hg38UCSC Ensembl
chr1:151898519..151899867hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381349
hg191349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325540
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