A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857459



Internal ID22041102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117718285..117718285hg38UCSC Ensembl
chr6:118039448..118039448hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257072
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857459
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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