A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855324



Internal ID22038967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15785551..15785551hg38UCSC Ensembl
chr4:15787174..15787174hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243778
Supporting Variants
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855324
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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