A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154629



Internal ID22085134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79259191..79263764hg38UCSC Ensembl
Outerchr10:79258505..79265861hg38UCSC Ensembl
Innerchr10:81018948..81023521hg19UCSC Ensembl
Outerchr10:81018262..81025618hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387357
hg197357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005998
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154629
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