A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574346



Internal ID16361755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10268563..10298798hg38UCSC Ensembl
Innerchr17:10171880..10202115hg19UCSC Ensembl
Innerchr17:10112605..10142840hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3830236
hg1930236
hg1830236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5444n54
Supporting Variantsnssv1149693
SamplesHGDP01244
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574346
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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