A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495877



Internal ID18736832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683008..109703496hg38UCSC Ensembl
Innerchr1:110225630..110246118hg19UCSC Ensembl
Innerchr1:110027153..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820489
hg1920489
hg1820489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010250
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)nssv3495877
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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