A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059895



Internal ID19149114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:23029488..23116708hg38UCSC Ensembl
Innerchr18:20609451..20696672hg19UCSC Ensembl
Innerchr18:18863449..18950670hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3887221
hg1987222
hg1887222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564136, nssv3564135
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)nsv1059895
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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