A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951268



Internal ID16953455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:368601..503700hg38UCSC Ensembl
Outerchr11:368601..503700hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38135100
hg19135100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998110
SamplesBILGI_BIOE
Known GenesANO9, B4GALNT4, PKP3, PTDSS2, RNH1, SIGIRR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951268
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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