A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838937



Internal ID22022580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162690653..162690653hg38UCSC Ensembl
chr1:162660443..162660443hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245338
Supporting Variants
Samples
Known GenesDDR2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838937
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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