A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131021



Internal ID18933076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14358654..14359154hg38UCSC Ensembl
Outerchr11:14380200..14380700hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967727
SamplesKWS2
Known GenesRRAS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131021
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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