A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156463



Internal ID22086864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26270381..26289082hg38UCSC Ensembl
Outerchr6:26265451..26289207hg38UCSC Ensembl
Innerchr6:26270609..26289310hg19UCSC Ensembl
Outerchr6:26265679..26289435hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3823757
hg1923757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018318
Samples
Known GenesHIST1H2BI, HIST1H3G, HIST1H4H
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156463
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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