A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848839



Internal ID22032482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32027260..32027260hg38UCSC Ensembl
chr17:30354279..30354279hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250738
Supporting Variants
Samples
Known GenesLRRC37B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848839
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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