A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247740



Internal ID22052350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7708646..7708646hg38UCSC Ensembl
chr11:7730193..7730193hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247740
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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