A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141792



Internal ID19277486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:66762924..66762999hg38UCSC Ensembl
Outerchr2:66990056..66990131hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1928n106
Supporting Variantsnssv3993298
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141792
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