A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124890



Internal ID19277224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49282883..49336783hg38UCSC Ensembl
Outerchr4:49284900..49338800hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3853901
hg1953901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977695
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124890
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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