A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951032



Internal ID17299906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:69593233..69597732hg38UCSC Ensembl
Outerchr11:69408001..69412500hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999579
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951032
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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