A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857408



Internal ID22041051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79014084..79014084hg38UCSC Ensembl
chr6:79723801..79723801hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256752
Supporting Variants
Samples
Known GenesPHIP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857408
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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