A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604146



Internal ID16391555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92390188..92418235hg38UCSC Ensembl
Innerchr6:93099906..93127953hg19UCSC Ensembl
Innerchr6:93156627..93184674hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3828048
hg1928048
hg1828048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10840n54
Supporting Variantsnssv1155763
Samples1780854495_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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