A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842704



Internal ID22026347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26196161..26196161hg38UCSC Ensembl
chr1:26522652..26522652hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258127
Supporting Variants
Samples
Known GenesCATSPER4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842704
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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