A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353582



Internal ID22281362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130150353..130150978hg38UCSC Ensembl
chrX:129284328..129284953hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202996
Supporting Variants
SamplesNA19239
Known GenesAIFM1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353582
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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