A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157689



Internal ID20724729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52479401..52479900hg38UCSC Ensembl
chr7:52547097..52547596hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00088


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer