A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065247



Internal ID20632287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9575443..9577244hg38UCSC Ensembl
chr1:9635501..9637302hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320455
Supporting Variants
Samples
Known GenesSLC25A33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065247
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