A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155488



Internal ID22085993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57100840..57108185hg38UCSC Ensembl
Outerchr17:57096744..57110686hg38UCSC Ensembl
Innerchr17:55178201..55185546hg19UCSC Ensembl
Outerchr17:55174105..55188047hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3813943
hg1913943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011868
Samples
Known GenesAKAP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155488
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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