A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574754



Internal ID16362163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35514718..35554612hg38UCSC Ensembl
Innerchr17:33841737..33881631hg19UCSC Ensembl
Innerchr17:30865850..30905744hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3839895
hg1939895
hg1839895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869854
Samples
Known GenesSLFN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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