A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850496



Internal ID22034139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41936508..41936508hg38UCSC Ensembl
chr2:42163648..42163648hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251461
Supporting Variants
Samples
Known GenesC2orf91
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850496
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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