A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527548



Internal ID15454841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29770771..29866221hg38UCSC Ensembl
InnerchrX:29788888..29884338hg19UCSC Ensembl
InnerchrX:29698809..29794259hg18UCSC Ensembl
InnerchrX:29548545..29643995hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3895451
hg1995451
hg1895451
hg1795451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704009
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527548
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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