A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951406



Internal ID22726768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31304589..31304589hg38UCSC Ensembl
chr2:31527455..31527455hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951406
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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