A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574752



Internal ID16362161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35404745..35433147hg38UCSC Ensembl
Innerchr17:33731764..33760166hg19UCSC Ensembl
Innerchr17:30755877..30784279hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3828403
hg1928403
hg1828403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5533n54
Supporting Variantsnssv869852
Samples
Known GenesSLFN12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574752
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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