A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601007



Internal ID16388416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:16018884..16055795hg38UCSC Ensembl
Innerchr6:16019115..16056026hg19UCSC Ensembl
Innerchr6:16127094..16164005hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3836912
hg1936912
hg1836912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153634
SamplesHGDP01336
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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