A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921076



Internal ID22696299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39754024..39754959hg38UCSC Ensembl
chr8:39611543..39612478hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441184
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921076
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer