A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857652



Internal ID22041295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:136586156..136586156hg38UCSC Ensembl
chr4:137507311..137507311hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857652
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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