A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252871



Internal ID22057481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113981343..113981343hg38UCSC Ensembl
chr2:114738920..114738920hg19UCSC Ensembl
Cytoband2q14.1
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 Variantsnssv17852547
Samples
Known GenesLOC440900
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252871
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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