A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239852



Internal ID22044462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142152475..142152475hg38UCSC Ensembl
chr7:141852275..141852275hg19UCSC Ensembl
Cytoband7q34
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 Variantsnssv17839342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239852
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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