A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522610



Internal ID15449903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29555905..29578747hg38UCSC Ensembl
InnerchrX:29574022..29596864hg19UCSC Ensembl
InnerchrX:29483943..29506785hg18UCSC Ensembl
InnerchrX:29333679..29356521hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3822843
hg1922843
hg1822843
hg1722843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706002
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522610
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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