A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447030



Internal ID22504900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99240045..99240045hg38UCSC Ensembl
chr7:98837668..98837668hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447030
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