A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110376



Internal ID19255756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9271267..9328067hg38UCSC Ensembl
Outerchr21:10110100..10166900hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3856801
hg1956801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960027
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110376
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