A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155370



Internal ID22085875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4388755..4892012hg38UCSC Ensembl
Outerchr17:4386079..4898009hg38UCSC Ensembl
Innerchr17:4292050..4795307hg19UCSC Ensembl
Outerchr17:4289374..4801304hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38511931
hg19511931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010078
Samples
Known GenesALOX15, ARRB2, CHRNE, CXCL16, GGT6, GLTPD2, LOC101559451, MED11, MINK1, MYBBP1A, PELP1, PLD2, PSMB6, SMTNL2, SPNS2, SPNS3, TM4SF5, VMO1, ZMYND15
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155370
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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