A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003229



Internal ID19092447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109676374..109710508hg38UCSC Ensembl
Innerchr1:110218996..110253130hg19UCSC Ensembl
Innerchr1:110020519..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3834135
hg1934135
hg1834135
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv263n100
Supporting Variantsnssv3489093, nssv3501636, nssv3492319, nssv3701171
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003229
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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