A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056012



Internal ID19145231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41079688..41093525hg38UCSC Ensembl
Innerchr18:38659652..38673489hg19UCSC Ensembl
Innerchr18:36913650..36927487hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3813838
hg1913838
hg1813838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565341
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)nsv1056012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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