A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067510



Internal ID19156729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14569387..14741639hg38UCSC Ensembl
Innerchr18:14569386..14741638hg19UCSC Ensembl
Innerchr18:14559386..14731638hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38172253
hg19172253
hg18172253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725294
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)nsv1067510
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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