A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446830



Internal ID22504700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63203916..63203965hg38UCSC Ensembl
chr6:63913821..63913870hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889394
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446830
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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