A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216691



Internal ID20783731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156504631..156505027hg38UCSC Ensembl
chr6:156825765..156826161hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216691
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