A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256424



Internal ID22061034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111960309..111960309hg38UCSC Ensembl
chr1:112502931..112502931hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856429
Samples
Known GenesKCND3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256424
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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