A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353288



Internal ID22208724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139963637..139963770hg38UCSC Ensembl
chrX:139045796..139045929hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526982
Supporting Variants
SamplesHG00732
Known GenesCXorf66
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353288
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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