A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661621



Internal ID15398273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28903390..29356165hg38UCSC Ensembl
InnerchrX:28921507..29374282hg19UCSC Ensembl
InnerchrX:28831428..29284203hg18UCSC Ensembl
InnerchrX:28681164..29133939hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38452776
hg19452776
hg18452776
hg17452776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516364
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661621
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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