A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347749



Internal ID21005302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163290792..163297507hg38UCSC Ensembl
chr2:164147302..164154017hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg386716
hg196716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347749
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