A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850145



Internal ID22033788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136186898..136186898hg38UCSC Ensembl
chrX:135269057..135269057hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242981
Supporting Variants
Samples
Known GenesFHL1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850145
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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