A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252524



Internal ID22057134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64707817..64707817hg38UCSC Ensembl
chr2:64934951..64934951hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252524
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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