A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067091



Internal ID19156310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74424482..74442193hg38UCSC Ensembl
Innerchr18:72091717..72109428hg19UCSC Ensembl
Innerchr18:70242697..70260408hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3817712
hg1917712
hg1817712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563025
Samples
Known GenesFAM69C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067091
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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