A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960076



Internal ID22735096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209827668..209827668hg38UCSC Ensembl
chr1:210001013..210001013hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960076
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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