A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156881



Internal ID20723921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20267349..20268054hg38UCSC Ensembl
chr7:20306972..20307677hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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