A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211707



Internal ID20778747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70021570..70034169hg38UCSC Ensembl
chr4:70887287..70899886hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3812600
hg1912600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378354
Supporting Variants
Samples
Known GenesHTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211707
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