A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001968



Internal ID19091185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690340..109707938hg38UCSC Ensembl
Innerchr1:110232962..110250560hg19UCSC Ensembl
Innerchr1:110034485..110052083hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817599
hg1917599
hg1817599
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n100
Supporting Variantsnssv3484255, nssv3702402
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)nsv1001968
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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