A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226451



Internal ID20793491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20428867..20536797hg38UCSC Ensembl
chr7:20468490..20576420hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38107931
hg19107931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer