A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397745



Internal ID177149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38312904..38312955hg38UCSC Ensembl
chr4:38314525..38314576hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397745
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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