A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843553



Internal ID22027196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8065195..8065195hg38UCSC Ensembl
chr12:8217791..8217791hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258600
Supporting Variants
Samples
Known GenesC3AR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843553
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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