A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156465



Internal ID22086866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26288019..26290439hg38UCSC Ensembl
Outerchr6:26286438..26291299hg38UCSC Ensembl
Innerchr6:26288247..26290667hg19UCSC Ensembl
Outerchr6:26286666..26291527hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg384862
hg194862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018320
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156465
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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