A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066698



Internal ID18809229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46092749..46276519hg38UCSC Ensembl
Innerchr17:44170115..44353885hg19UCSC Ensembl
Innerchr17:41525932..41709662hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38183771
hg19183771
hg18183731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3194n100
Supporting Variantsnssv3720536
Samples
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066698
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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