A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097264



Internal ID22006497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39937287..39937287hg38UCSC Ensembl
chr15:40229488..40229488hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602864
Samples
Known GenesEIF2AK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097264
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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