A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439078



Internal ID21096631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80272101..80272900hg38UCSC Ensembl
chr9:82887016..82887815hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439078
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