A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615709



Internal ID20988780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82143327..82143969hg38UCSC Ensembl
chr7:81772643..81773285hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160304
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615709
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