A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855663



Internal ID22039306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140659170..140659170hg38UCSC Ensembl
chr5:140038755..140038755hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244896
Supporting Variants
Samples
Known GenesIK
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855663
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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