A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203566



Internal ID22352550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29476722..29476891hg38UCSC Ensembl
chrX:29494839..29495008hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350776
SamplesNA19239
Known GenesIL1RAPL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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