A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104026



Internal ID21280554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29581953..29590784hg38UCSC Ensembl
InnerchrX:29600070..29608901hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg388832
hg198832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117545
Supporting Variants
Samplessample3
Known GenesIL1RAPL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104026
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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