A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155576



Internal ID20722616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26229303..26235187hg38UCSC Ensembl
chr7:26268923..26274807hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg385885
hg195885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155576
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