A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002827



Internal ID18745359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684336..109714002hg38UCSC Ensembl
Innerchr1:110226958..110256624hg19UCSC Ensembl
Innerchr1:110028481..110058147hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3829667
hg1929667
hg1829667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv273n100
Supporting Variantsnssv3498708, nssv3501152
Samples
Known GenesGSTM1, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002827
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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