A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951011



Internal ID17299885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64625429..64655928hg38UCSC Ensembl
Outerchr11:64392901..64423400hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3830500
hg1930500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999559
SamplesBILGI_BIOE
Known GenesNRXN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951011
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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