A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858099



Internal ID22041742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1044014..1044014hg38UCSC Ensembl
chr7:1083650..1083650hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6261004
Supporting Variants
Samples
Known GenesC7orf50
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858099
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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