A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999584



Internal ID16945850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72000055..72016354hg38UCSC Ensembl
Outerchr11:71711101..71727400hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3816300
hg1916300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951037
Supporting Variants
SamplesBILGI_BIOE
Known GenesIL18BP, LOC100128494, NUMA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999584
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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