A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527992



Internal ID15455285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29620161..29673400hg38UCSC Ensembl
InnerchrX:29638278..29691517hg19UCSC Ensembl
InnerchrX:29548199..29601438hg18UCSC Ensembl
InnerchrX:29397935..29451174hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3853240
hg1953240
hg1853240
hg1753240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704515
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527992
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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