A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068446



Internal ID20635486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47681948..47682154hg38UCSC Ensembl
chr20:46310692..46310898hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554103
Supporting Variants
Samples
Known GenesSULF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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