A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970689



Internal ID22745624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35578409..35578409hg38UCSC Ensembl
chr22:35974456..35974456hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970689
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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