A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142241



Internal ID20709281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32966429..32967039hg38UCSC Ensembl
chr6:32934206..32934816hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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