A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066298



Internal ID18808829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46142189..46203331hg38UCSC Ensembl
Innerchr17:44219555..44280697hg19UCSC Ensembl
Innerchr17:41575332..41636474hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3861143
hg1961143
hg1861143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3216n100
Supporting Variantsnssv3556697, nssv3556698
Samples
Known GenesKANSL1, KANSL1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066298
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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