A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528242



Internal ID15108849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139560234..139590536hg38UCSC Ensembl
InnerchrX:138642393..138672695hg19UCSC Ensembl
InnerchrX:138470059..138500361hg18UCSC Ensembl
InnerchrX:138367913..138398215hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3830303
hg1930303
hg1830303
hg1730303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704804
Samples
Known GenesF9, MCF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528242
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