A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519107



Internal ID15446400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34926881..35018962hg38UCSC Ensembl
InnerchrX:34944998..35037079hg19UCSC Ensembl
InnerchrX:34854919..34947000hg18UCSC Ensembl
InnerchrX:34704655..34796736hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3892082
hg1992082
hg1892082
hg1792082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696583
Samples
Known GenesFAM47B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519107
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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