A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960715



Internal ID22649563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22890891..22890891hg38UCSC Ensembl
chr2:23113763..23113763hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960715
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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