A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849006



Internal ID22032649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73651167..73651167hg38UCSC Ensembl
chr17:71647306..71647306hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849006
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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