A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502478



Internal ID22560418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155844841..155855166hg38UCSC Ensembl
chr6:156165975..156176300hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810326
hg1910326
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502478
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