A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424949



Internal ID21082502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50665801..50679000hg38UCSC Ensembl
chr8:51578361..51591560hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7336n223
Supporting Variantsnssv18167584
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424949
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