A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851901



Internal ID22035544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110330036..110330036hg38UCSC Ensembl
chrX:109573264..109573264hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259695
Supporting Variants
Samples
Known GenesAMMECR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851901
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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