A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852275



Internal ID22035918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42873308..42873308hg38UCSC Ensembl
chr1:43338979..43338979hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252770
Supporting Variants
Samples
Known GenesLOC339539
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852275
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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