A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064540



Internal ID19153759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9995048..10133807hg38UCSC Ensembl
Innerchr18:9995045..10133804hg19UCSC Ensembl
Innerchr18:9985045..10123804hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38138760
hg19138760
hg18138760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3320n100
Supporting Variantsnssv3564099
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064540
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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