A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954477



Internal ID22729715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67862591..67862591hg38UCSC Ensembl
chr2:68089723..68089723hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954477
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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