A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436573



Internal ID22494443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109337068..109337068hg38UCSC Ensembl
chr8:110349297..110349297hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952007
Supporting Variants
Samples
Known GenesENY2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436573
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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