A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958247



Internal ID22733321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3293967..3293967hg38UCSC Ensembl
chr4:3295694..3295694hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958247
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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