A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853189



Internal ID22036832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53771926..53771926hg38UCSC Ensembl
chr1:54237599..54237599hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253350
Supporting Variants
Samples
Known GenesNDC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853189
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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