A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011882



Internal ID18754417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87442807..87481325hg38UCSC Ensembl
Innerchr4:88363959..88402477hg19UCSC Ensembl
Innerchr4:88582983..88621501hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3838519
hg1938519
hg1838519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633929
Samples
Known GenesNUDT9, SPARCL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011882
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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