A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522699



Internal ID15103306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131270380..131288648hg38UCSC Ensembl
InnerchrX:130404354..130422622hg19UCSC Ensembl
InnerchrX:130232035..130250303hg18UCSC Ensembl
InnerchrX:130129889..130148157hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3818269
hg1918269
hg1818269
hg1718269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706110
Samples
Known GenesIGSF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522699
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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