A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5395714



Internal ID175136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8862596..8862647hg38UCSC Ensembl
chr1:8922655..8922706hg19UCSC Ensembl
Cytoband1p36.23
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 Variantsnssv16889436
Samples
Known GenesENO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5395714
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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