A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839359



Internal ID22023002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173657644..173657644hg38UCSC Ensembl
chr1:173626783..173626783hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245613
Supporting Variants
Samples
Known GenesANKRD45
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839359
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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