A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018308



Internal ID22079939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4170292..4174062hg38UCSC Ensembl
Outerchr6:4167285..4177293hg38UCSC Ensembl
Innerchr6:4170526..4174296hg19UCSC Ensembl
Outerchr6:4167519..4177527hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3810009
hg1910009
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156454
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018308
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