A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155427



Internal ID22085932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41376617..41380422hg38UCSC Ensembl
Outerchr17:41372886..41391076hg38UCSC Ensembl
Innerchr17:39532869..39536674hg19UCSC Ensembl
Outerchr17:39529138..39547328hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3818191
hg1918191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010635, nssv4010634
Samples
Known GenesKRT34
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155427
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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