A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999544



Internal ID16945810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55597925..55664024hg38UCSC Ensembl
Outerchr11:55365401..55431500hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3866100
hg1966100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952449
Supporting Variants
SamplesBILGI_BIOE
Known GenesOR4C11, OR4P4, OR4S2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999544
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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