A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999588



Internal ID16945854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:73336156..73402655hg38UCSC Ensembl
Outerchr11:73047201..73113700hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3866500
hg1966500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951041
Supporting Variants
SamplesBILGI_BIOE
Known GenesARHGEF17, FAM168A, RELT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999588
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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