A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005251



Internal ID18747782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690403..109703496hg38UCSC Ensembl
Innerchr1:110233025..110246118hg19UCSC Ensembl
Innerchr1:110034548..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3813094
hg1913094
hg1813094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv274n100
Supporting Variantsnssv3486685, nssv3502318, nssv3501944, nssv3490110, nssv3488328, nssv3491655, nssv3498897
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)nsv1005251
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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