A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063343



Internal ID19152562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42180979..42318533hg38UCSC Ensembl
Innerchr18:39760943..39898498hg19UCSC Ensembl
Innerchr18:38014941..38152496hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38137555
hg19137556
hg18137556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725323
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)nsv1063343
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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