A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354169



Internal ID22234207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148389589..148389589hg38UCSC Ensembl
chrX:147471109..147471109hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565953
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354169
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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