A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120664



Internal ID18914108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132688744..132689015hg38UCSC Ensembl
Outerchr11:132558639..132558910hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv740n106
Supporting Variantsnssv3963095
SamplesKWS2
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120664
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