A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999988



Internal ID19159524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683286..109694313hg38UCSC Ensembl
Innerchr1:110225908..110236935hg19UCSC Ensembl
Innerchr1:110027431..110038458hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3811028
hg1911028
hg1811028
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv266n100
Supporting Variantsnssv3499627, nssv3482908
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)nsv999988
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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