A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261236



Internal ID22065846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29941131..29941131hg38UCSC Ensembl
chr7:29980747..29980747hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859981
Samples
Known GenesSCRN1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261236
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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