A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418605



Internal ID21076158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139446549..139453373hg38UCSC Ensembl
chr7:139131295..139138119hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386825
hg196825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155259
Samples
Known GenesKLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418605
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