A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004021



Internal ID18746552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109638683..109691994hg38UCSC Ensembl
Innerchr1:110181305..110234616hg19UCSC Ensembl
Innerchr1:109982828..110036139hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3853312
hg1953312
hg1853312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv256n100
Supporting Variantsnssv3487547
Samples
Known GenesGSTM1, GSTM2, GSTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004021
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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