A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604735



Internal ID16392144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137218368..137220160hg38UCSC Ensembl
Innerchr6:137539505..137541297hg19UCSC Ensembl
Innerchr6:137581198..137582990hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381793
hg191793
hg181793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073593
Samples
Known GenesIFNGR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604735
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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