A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851634



Internal ID22035277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55892455..55892455hg38UCSC Ensembl
chr2:56119590..56119590hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252437
Supporting Variants
Samples
Known GenesEFEMP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851634
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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