A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018818



Internal ID19108035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169624445..169671797hg38UCSC Ensembl
Innerchr6:170024541..170071893hg19UCSC Ensembl
Innerchr6:169766466..169813818hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3847353
hg1947353
hg1847353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653092
Samples
Known GenesWDR27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018818
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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