A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858768



Internal ID22042411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12101950..12101950hg38UCSC Ensembl
chr6:12102183..12102183hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256655
Supporting Variants
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858768
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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