A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066669



Internal ID19155888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40237274..40269920hg38UCSC Ensembl
Innerchr18:37817238..37849884hg19UCSC Ensembl
Innerchr18:36071236..36103882hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3832647
hg1932647
hg1832647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3339n100
Supporting Variantsnssv3565330
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)nsv1066669
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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