A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853444



Internal ID22037087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237235084..237235084hg38UCSC Ensembl
chr2:238143727..238143727hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853444
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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