A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431440



Internal ID21088993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10056185..10058546hg38UCSC Ensembl
chr8:9913695..9916056hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161357
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431440
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