A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066863



Internal ID19156082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77649960..77666415hg38UCSC Ensembl
Innerchr18:75361916..75378371hg19UCSC Ensembl
Innerchr18:73490904..73507359hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3816456
hg1916456
hg1816456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563044
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)nsv1066863
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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