A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999561



Internal ID16945827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64777329..64847128hg38UCSC Ensembl
Outerchr11:64544801..64614600hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3869800
hg1969800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951013
Supporting Variants
SamplesBILGI_BIOE
Known GenesCDC42BPG, MAP4K2, MEN1, SF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999561
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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