A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506447



Internal ID22564394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51504263..51506246hg38UCSC Ensembl
chr6:51369061..51371044hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381984
hg191984
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506447
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