A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156057



Internal ID22086562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180428989..180447317hg38UCSC Ensembl
Outerchr3:180418034..180453756hg38UCSC Ensembl
Innerchr3:180146777..180165105hg19UCSC Ensembl
Outerchr3:180135822..180171544hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3835723
hg1935723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017221
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156057
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer