A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353065



Internal ID22265739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95713603..95713603hg38UCSC Ensembl
chrX:94968602..94968602hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565610
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353065
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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