A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199615



Internal ID21338411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95824119..95824238hg38UCSC Ensembl
chr8:96836347..96836466hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937303
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199615
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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