A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156495



Internal ID22086896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37995532..38018691hg38UCSC Ensembl
Outerchr6:37993807..38020088hg38UCSC Ensembl
Innerchr6:37963308..37986467hg19UCSC Ensembl
Outerchr6:37961583..37987864hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3826282
hg1926282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018552
Samples
Known GenesZFAND3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156495
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