A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160280



Internal ID20727320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82021287..82021653hg38UCSC Ensembl
chr7:81650603..81650969hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619385
Supporting Variants
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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