A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014873



Internal ID19104090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690340..109710508hg38UCSC Ensembl
Innerchr1:110232962..110253130hg19UCSC Ensembl
Innerchr1:110034485..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820169
hg1920169
hg1820169
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n100
Supporting Variantsnssv3702408, nssv3702407, nssv3702406, nssv3484431, nssv3492391, nssv3500968, nssv3498078, nssv3483198, nssv3499406, nssv3489644, nssv3494313
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014873
Frequency
Sample Size11257
Observed Gain4
Observed Loss7
Observed Complex0
Frequencyn/a


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