A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155380



Internal ID22085885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15773687..15791471hg38UCSC Ensembl
Outerchr17:15770691..15791687hg38UCSC Ensembl
Innerchr17:15677001..15694785hg19UCSC Ensembl
Outerchr17:15674005..15695001hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820997
hg1920997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010109, nssv4010110
Samples
Known GenesMEIS3P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155380
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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