A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611985



Internal ID20985056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11873821..11904735hg38UCSC Ensembl
chr7:11913447..11944361hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3830915
hg1930915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611985
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