A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951600



Internal ID16953787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:34136054..34174953hg38UCSC Ensembl
Outerchr11:34157601..34196500hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3838900
hg1938900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998173
SamplesBILGI_BIOE
Known GenesABTB2, NAT10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951600
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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