A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612092



Internal ID20985163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2346401..2351900hg38UCSC Ensembl
chr7:2386036..2391535hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6540n223
Supporting Variantsnssv18154922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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