A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843032



Internal ID22026675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47256671..47256671hg38UCSC Ensembl
chr11:47278222..47278222hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248056
Supporting Variants
Samples
Known GenesNR1H3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843032
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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