A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853008



Internal ID22036651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98491611..98491611hg38UCSC Ensembl
chr2:99108074..99108074hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252762
Supporting Variants
Samples
Known GenesINPP4A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853008
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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