A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155399



Internal ID22085904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36108119..36215889hg38UCSC Ensembl
Outerchr17:36103057..36258784hg38UCSC Ensembl
Innerchr17:34435512..34543343hg19UCSC Ensembl
Outerchr17:34430450..34586294hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38155728
hg19155845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv129n97
Supporting Variantsnssv4010183
Samples
Known GenesCCL3L1, CCL3L3, CCL4, CCL4L1, CCL4L2, TBC1D3B, TBC1D3H
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155399
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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