A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249863



Internal ID22054473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80813680..80813680hg38UCSC Ensembl
chr15:81106021..81106021hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848696
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249863
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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