A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851510



Internal ID22035153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23841472..23841472hg38UCSC Ensembl
chrX:23859589..23859589hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252370
Supporting Variants
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851510
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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