A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446545



Internal ID22504415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108467747..108467747hg38UCSC Ensembl
chr7:108108191..108108191hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446545
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