A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842951



Internal ID22026594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84179892..84179892hg38UCSC Ensembl
chr10:85939648..85939648hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247316
Supporting Variants
Samples
Known GenesC10orf99
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842951
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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