A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596169



Internal ID16383578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171042082..171573082hg38UCSC Ensembl
Innerchr4:171963233..172494233hg19UCSC Ensembl
Innerchr4:172199808..172730808hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38531001
hg19531001
hg18531001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1013117
Samples
Known GenesLOC100506122, MIR6082
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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