A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999589



Internal ID17292541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:75098156..75099955hg38UCSC Ensembl
Outerchr11:74809201..74811000hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951042
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999589
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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