A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051356



Internal ID15557856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24632414..24665779hg38UCSC Ensembl
Innerchr6:24632642..24666007hg19UCSC Ensembl
Innerchr6:24740621..24773986hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3833366
hg1933366
hg1833366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601165
Supporting Variants
Samples
Known GenesKIAA0319, TDP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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