A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856079



Internal ID22039722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145622858..145622858hg38UCSC Ensembl
chr4:146544010..146544010hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255464
Supporting Variants
Samples
Known GenesMMAA
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856079
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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