A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520008



Internal ID15447301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152914199..152966404hg38UCSC Ensembl
InnerchrX:152082743..152134948hg19UCSC Ensembl
InnerchrX:151833399..151885604hg18UCSC Ensembl
InnerchrX:151753311..151805516hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3852206
hg1952206
hg1852206
hg1752206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697175
Samples
Known GenesZNF185
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520008
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