A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963276



Internal ID22738211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117837052..117837052hg38UCSC Ensembl
chr1:118379674..118379674hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963276
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