A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348598



Internal ID21006151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163697345..163697832hg38UCSC Ensembl
chr2:164553855..164554342hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079599
Samples
Known GenesFIGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348598
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