A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574352



Internal ID16361761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10984945..10996377hg38UCSC Ensembl
Innerchr17:10888262..10899694hg19UCSC Ensembl
Innerchr17:10828987..10840419hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3811433
hg1911433
hg1811433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149695
SamplesHGDP00954
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574352
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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