A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501081



Internal ID22559018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114346134..114357729hg38UCSC Ensembl
chr6:114667298..114678893hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3811596
hg1911596
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501081
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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