A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352703



Internal ID22280406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120296566..120297169hg38UCSC Ensembl
chrX:119430421..119431024hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525951
Supporting Variants
SamplesNA19239
Known GenesTMEM255A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352703
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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