A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574523



Internal ID16361932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17407572..17444681hg38UCSC Ensembl
Innerchr17:17310886..17347995hg19UCSC Ensembl
Innerchr17:17251611..17288720hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3837110
hg1937110
hg1837110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868857
Samples
Known GenesSMCR9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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