A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604734



Internal ID16392143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137218368..137219938hg38UCSC Ensembl
Innerchr6:137539505..137541075hg19UCSC Ensembl
Innerchr6:137581198..137582768hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381571
hg191571
hg181571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073592
Samples
Known GenesIFNGR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604734
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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