A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997826



Internal ID20564866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121979860..121982586hg38UCSC Ensembl
chr12:122417766..122420492hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382727
hg192727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484886
Supporting Variants
Samples
Known GenesWDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997826
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