A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156577



Internal ID22086978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118280163..118461942hg38UCSC Ensembl
Outerchr6:118279883..118464251hg38UCSC Ensembl
Innerchr6:118601326..118783105hg19UCSC Ensembl
Outerchr6:118601046..118785414hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38184369
hg19184369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022627
Samples
Known GenesCEP85L, SLC35F1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156577
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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