A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3653092



Internal ID18951373
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 StatusS
Merged Variantsnsv1018818
Supporting Variants
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)nssv3653092
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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