A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197632



Internal ID22347487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104853626..104853920hg38UCSC Ensembl
chrX:104098306..104098600hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353182, nssv14353181
SamplesNA19240, HG00733
Known GenesIL1RAPL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197632
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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