A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064907



Internal ID19154126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15249168..15401752hg38UCSC Ensembl
Innerchr18:15249167..15401751hg19UCSC Ensembl
Innerchr18:15239167..15391751hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg38152585
hg19152585
hg18152585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564124
Samples
Known GenesLOC644669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064907
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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