A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156464



Internal ID22086865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26270381..26292219hg38UCSC Ensembl
Outerchr6:26265451..26302950hg38UCSC Ensembl
Innerchr6:26270609..26292447hg19UCSC Ensembl
Outerchr6:26265679..26303178hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3837500
hg1937500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018319
Samples
Known GenesHIST1H2BI, HIST1H3G, HIST1H4H
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156464
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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