A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000913



Internal ID19090130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109677464..109703496hg38UCSC Ensembl
Innerchr1:110220086..110246118hg19UCSC Ensembl
Innerchr1:110021609..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3826033
hg1926033
hg1826033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv264n100
Supporting Variantsnssv3485247
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)nsv1000913
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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