A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169034



Internal ID20736074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39373201..39529700hg38UCSC Ensembl
chr8:39230720..39387219hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38156500
hg19156500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426776
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.37065


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