A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354923



Internal ID22316447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154831507..154831782hg38UCSC Ensembl
chrX:154059782..154060057hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525870
Supporting Variants
SamplesNA19240
Known GenesSMIM9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354923
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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