A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003418



Internal ID18745949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683506..109694313hg38UCSC Ensembl
Innerchr1:110226128..110236935hg19UCSC Ensembl
Innerchr1:110027651..110038458hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810808
hg1910808
hg1810808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv271n100
Supporting Variantsnssv3488497, nssv3495720, nssv3499568, nssv3493705
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)nsv1003418
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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