A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006541



Internal ID18749072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109676374..109692410hg38UCSC Ensembl
Innerchr1:110218996..110235032hg19UCSC Ensembl
Innerchr1:110020519..110036555hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3816037
hg1916037
hg1816037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv260n100
Supporting Variantsnssv3488804
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)nsv1006541
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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