A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155989



Internal ID22086494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75745416..76340979hg38UCSC Ensembl
Outerchr3:75742905..76350048hg38UCSC Ensembl
Innerchr3:75794567..76390130hg19UCSC Ensembl
Outerchr3:75792056..76399199hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38607144
hg19607144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017625
Samples
Known GenesZNF717
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155989
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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