A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998022



Internal ID18810872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109650144..109703496hg38UCSC Ensembl
Innerchr1:110192766..110246118hg19UCSC Ensembl
Innerchr1:109994289..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3853353
hg1953353
hg1853353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv255n100
Supporting Variantsnssv3500197, nssv3484269
Samples
Known GenesGSTM1, GSTM2, GSTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998022
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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