A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062149



Internal ID19151368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12728116..12783899hg38UCSC Ensembl
Innerchr18:12728115..12783898hg19UCSC Ensembl
Innerchr18:12718115..12773898hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3855784
hg1955784
hg1855784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725292
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)nsv1062149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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