A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601311



Internal ID16042034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891740..29908663hg38UCSC Ensembl
Innerchr6:29859517..29876440hg19UCSC Ensembl
Innerchr6:29967496..29984419hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3816924
hg1916924
hg1816924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10351n54
Supporting Variantsnssv1051879, nssv1051880, nssv1051881, nssv1051878, nssv1051877
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601311
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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