A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353855



Internal ID22209003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107611303..107611712hg38UCSC Ensembl
chrX:106854533..106854942hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206009
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353855
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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