A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604554



Internal ID16045277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118310119..118395155hg38UCSC Ensembl
Innerchr6:118631282..118716318hg19UCSC Ensembl
Innerchr6:118737975..118823011hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3885037
hg1985037
hg1885037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072346
Samples
Known GenesSLC35F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604554
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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