A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952459



Internal ID16954646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61712829..61788728hg38UCSC Ensembl
Outerchr11:61480301..61556200hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3875900
hg1975900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999554
SamplesBILGI_BIOE
Known GenesDAGLA, DKFZP434K028, MYRF
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952459
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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