A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003387



Internal ID20570427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73852127..73864676hg38UCSC Ensembl
chr12:74245907..74258456hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3812550
hg1912550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003387
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