A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261196



Internal ID22065806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24681542..24681542hg38UCSC Ensembl
chr7:24721161..24721161hg19UCSC Ensembl
Cytoband7p15.3
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 Variantsnssv17859937
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261196
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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