A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064665



Internal ID19153884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27794789..27849270hg38UCSC Ensembl
Innerchr18:25374753..25429234hg19UCSC Ensembl
Innerchr18:23628751..23683232hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3854482
hg1954482
hg1854482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564143
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)nsv1064665
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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