A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156617



Internal ID22087018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168472373..168477203hg38UCSC Ensembl
Outerchr6:168469779..168477860hg38UCSC Ensembl
Innerchr6:168873053..168877883hg19UCSC Ensembl
Outerchr6:168870459..168878540hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388082
hg198082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022835
Samples
Known GenesSMOC2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156617
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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