A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697388



Internal ID15434040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114981600..115071767hg38UCSC Ensembl
InnerchrX:114216163..114306330hg19UCSC Ensembl
InnerchrX:114122419..114212586hg18UCSC Ensembl
InnerchrX:114039143..114129310hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3890168
hg1990168
hg1890168
hg1790168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516624
Supporting Variants
Samples
Known GenesIL13RA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697388
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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