A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851574



Internal ID22035217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73976378..73976378hg38UCSC Ensembl
chrX:73196213..73196213hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259530
Supporting Variants
Samples
Known GenesJPX
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851574
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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