A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013959



Internal ID19103178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109677956..109697544hg38UCSC Ensembl
Innerchr1:110220578..110240166hg19UCSC Ensembl
Innerchr1:110022101..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819589
hg1919589
hg1819589
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262n100
Supporting Variantsnssv3701174, nssv3490085, nssv3701176, nssv3498528, nssv3701175
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)nsv1013959
Frequency
Sample Size11257
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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