A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353335



Internal ID22233489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141906090..141906301hg38UCSC Ensembl
chrX:140993876..140994087hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199715
Supporting Variants
SamplesHG00733
Known GenesMAGEC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353335
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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