A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615022



Internal ID20988093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20166163..20166686hg38UCSC Ensembl
chr7:20205786..20206309hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156872
Samples
Known GenesMACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615022
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