A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495720



Internal ID18736675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683506..109694313hg38UCSC Ensembl
Innerchr1:110226128..110236935hg19UCSC Ensembl
Innerchr1:110027651..110038458hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810808
hg1910808
hg1810808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003418
Supporting Variants
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)nssv3495720
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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