A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239849



Internal ID22044459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141783308..141783308hg38UCSC Ensembl
chr7:141483108..141483108hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239849
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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