A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322869



Internal ID20855984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115851209..115880805hg38UCSC Ensembl
chr1:116393830..116423426hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3829597
hg1929597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322869
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