A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601209



Internal ID16041932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27881898..27901543hg38UCSC Ensembl
Innerchr6:27849676..27869321hg19UCSC Ensembl
Innerchr6:27957655..27977300hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3819646
hg1919646
hg1819646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051655
Samples
Known GenesHIST1H2AM, HIST1H2BO, HIST1H3J
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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