A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251887



Internal ID22056497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37210707..37210707hg38UCSC Ensembl
chr21:38583008..38583008hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850689
Samples
Known GenesDSCR9
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251887
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer