A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596170



Internal ID16383579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171168136..171226746hg38UCSC Ensembl
Innerchr4:172089287..172147897hg19UCSC Ensembl
Innerchr4:172325862..172384472hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3858611
hg1958611
hg1858611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153516
SamplesHGDP01347
Known GenesMIR6082
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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