A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430169



Internal ID21087722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39083219..39083869hg38UCSC Ensembl
chr8:38940738..38941388hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169002
Samples
Known GenesADAM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430169
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