A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1073594



Internal ID15926780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137219198..137220160hg38UCSC Ensembl
Innerchr6:137540335..137541297hg19UCSC Ensembl
Innerchr6:137582028..137582990hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38963
hg19963
hg18963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604736
Supporting Variants
Samples
Known GenesIFNGR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1073594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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