A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024297



Internal ID20591337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25872618..25877639hg38UCSC Ensembl
chr15:26117765..26122786hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024297
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