A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351838



Internal ID22264272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57648498..57648498hg38UCSC Ensembl
chrX:57674931..57674931hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565842
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351838
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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