A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951598



Internal ID17300472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:32426455..32438354hg38UCSC Ensembl
Outerchr11:32448001..32459900hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998171
SamplesBILGI_BIOE
Known GenesWT1, WT1-AS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951598
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