A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051657



Internal ID15558157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28515705..28553539hg38UCSC Ensembl
Innerchr6:28483482..28521316hg19UCSC Ensembl
Innerchr6:28591461..28629295hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3837835
hg1937835
hg1837835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601211
Supporting Variants
Samples
Known GenesGPX5, GPX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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