A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857695



Internal ID22041338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172363029..172363029hg38UCSC Ensembl
chr4:173284180..173284180hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255720
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857695
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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