A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252496



Internal ID22057106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61530743..61530743hg38UCSC Ensembl
chr2:61757878..61757878hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850173
Samples
Known GenesXPO1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252496
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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