A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143248



Internal ID20710288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17306297..17313197hg38UCSC Ensembl
chr6:17306528..17313428hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386901
hg196901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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