A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520636



Internal ID15101243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40098436..40107944hg38UCSC Ensembl
Innerchr17:38254689..38264197hg19UCSC Ensembl
Innerchr17:35508215..35517723hg18UCSC Ensembl
Innerchr17:35508215..35517723hg17UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg389509
hg199509
hg189509
hg179509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673397, nssv679044
Samples
Known GenesNR1D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520636
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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