A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843140



Internal ID22026783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1741712..1741712hg38UCSC Ensembl
chr12:1850878..1850878hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258545
Supporting Variants
Samples
Known GenesADIPOR2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843140
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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