A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008867



Internal ID18751398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690403..109707602hg38UCSC Ensembl
Innerchr1:110233025..110250224hg19UCSC Ensembl
Innerchr1:110034548..110051747hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817200
hg1917200
hg1817200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv276n100
Supporting Variantsnssv3484480, nssv3494214, nssv3500397
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)nsv1008867
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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