A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352736



Internal ID22280447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120566346..120567141hg38UCSC Ensembl
chrX:119700201..119700996hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208105
Supporting Variants
SamplesNA19239
Known GenesCUL4B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352736
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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