A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422443



Internal ID21079996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145910401..145911200hg38UCSC Ensembl
chr7:145607494..145608293hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422443
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