A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202117



Internal ID20769157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96556222..96561773hg38UCSC Ensembl
chr1:97021778..97027329hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg385552
hg195552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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