A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433136



Internal ID21090689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84790073..84803459hg38UCSC Ensembl
chr8:85702308..85715694hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3813387
hg1913387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172002
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433136
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