A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239477



Internal ID22044087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95513333..95513333hg38UCSC Ensembl
chr7:95142645..95142645hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17838394
Samples
Known GenesASB4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239477
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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