A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055804



Internal ID19145023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70387974..70511409hg38UCSC Ensembl
Innerchr18:68055210..68178645hg19UCSC Ensembl
Innerchr18:66206190..66329625hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38123436
hg19123436
hg18123436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723213
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)nsv1055804
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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