A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848701



Internal ID22032344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81239794..81239794hg38UCSC Ensembl
chr15:81532135..81532135hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249868
Supporting Variants
Samples
Known GenesIL16
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848701
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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