A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152645



Internal ID20719685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12698811..12699568hg38UCSC Ensembl
chr7:12738436..12739193hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152645
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