A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031922



Internal ID19121144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39066708..39092986hg38UCSC Ensembl
Innerchr6:39034484..39060762hg19UCSC Ensembl
Innerchr6:39142462..39168740hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3826279
hg1926279
hg1826279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657430
Samples
Known GenesGLP1R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031922
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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