A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601145



Internal ID16388554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24052298..24080142hg38UCSC Ensembl
Innerchr6:24052526..24080370hg19UCSC Ensembl
Innerchr6:24160505..24188349hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3827845
hg1927845
hg1827845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154033
SamplesHGDP01341
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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