A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451371



Internal ID21108924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124809948..124814756hg38UCSC Ensembl
chr10:126498517..126503325hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384809
hg194809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978030
Samples
Known GenesFAM175B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451371
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