A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526653



Internal ID15107260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:120029666..120140727hg38UCSC Ensembl
InnerchrX:119163631..119274634hg19UCSC Ensembl
InnerchrX:119047659..119158662hg18UCSC Ensembl
InnerchrX:118945513..119056516hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38111062
hg19111004
hg18111004
hg17111004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702981
Samples
Known GenesRHOXF1, RHOXF2, RHOXF2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526653
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer