A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209558



Internal ID20776598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112771372..112799083hg38UCSC Ensembl
chr4:113692528..113720239hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3827712
hg1927712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209558
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