A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155485



Internal ID22085990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54595523..54625389hg38UCSC Ensembl
Outerchr17:54588492..54625488hg38UCSC Ensembl
Innerchr17:52672884..52702750hg19UCSC Ensembl
Outerchr17:52665853..52702849hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3836997
hg1936997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011864
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155485
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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