A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551989



Internal ID325406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142204896..142204937hg38UCSC Ensembl
chr6:142526033..142526074hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970311
Samples
Known GenesVTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551989
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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