A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847955



Internal ID22031598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37092730..37092730hg38UCSC Ensembl
chr15:37384931..37384931hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241933
Supporting Variants
Samples
Known GenesMEIS2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847955
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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