A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407944



Internal ID187274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224406804..224406855hg38UCSC Ensembl
chr1:224594506..224594557hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897221
Samples
Known GenesWDR26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407944
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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