A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239515



Internal ID22044125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103226577..103226577hg38UCSC Ensembl
chr7:102867024..102867024hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17838716
Samples
Known GenesDPY19L2P2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239515
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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