A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497389



Internal ID18738344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109650144..109694313hg38UCSC Ensembl
Innerchr1:110192766..110236935hg19UCSC Ensembl
Innerchr1:109994289..110038458hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3844170
hg1944170
hg1844170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014168
Supporting Variants
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)nssv3497389
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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