A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013410



Internal ID19102628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681750..109697521hg38UCSC Ensembl
Innerchr1:110224372..110240143hg19UCSC Ensembl
Innerchr1:110025895..110041666hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3815772
hg1915772
hg1815772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv268n100
Supporting Variantsnssv3497213
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)nsv1013410
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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