A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420093



Internal ID21077646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158330176..158341638hg38UCSC Ensembl
chr7:158122868..158134330hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811463
hg1911463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7204n223
Supporting Variantsnssv18152159
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420093
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