A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155603



Internal ID22086108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50858501..51111673hg38UCSC Ensembl
Outerchr19:50855858..51117057hg38UCSC Ensembl
Innerchr19:51361757..51614930hg19UCSC Ensembl
Outerchr19:51359114..51620314hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38261200
hg19261201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013661
Samples
Known GenesCTU1, KLK10, KLK11, KLK12, KLK13, KLK14, KLK2, KLK3, KLK4, KLK5, KLK6, KLK7, KLK8, KLK9, KLKP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155603
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