A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700121



Internal ID15436773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28903390..28964893hg38UCSC Ensembl
InnerchrX:28921507..28983010hg19UCSC Ensembl
InnerchrX:28831428..28892931hg18UCSC Ensembl
InnerchrX:28681164..28742667hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3861504
hg1961504
hg1861504
hg1761504
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)nssv700121
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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