A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057487



Internal ID19146706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65611615..65691239hg38UCSC Ensembl
Innerchr18:63278851..63358475hg19UCSC Ensembl
Innerchr18:61429831..61509455hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3879625
hg1979625
hg1879625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565645
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)nsv1057487
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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