A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415725



Internal ID21073278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36208901..36218600hg38UCSC Ensembl
chr8:36066419..36076118hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415725
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