A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055614



Internal ID19144833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42469073..42482352hg38UCSC Ensembl
Innerchr18:40049038..40062317hg19UCSC Ensembl
Innerchr18:38303036..38316315hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3813280
hg1913280
hg1813280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725326, nssv3725327
Samples
Known GenesLINC00907
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055614
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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