A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998154



Internal ID16944420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14524455..14526654hg38UCSC Ensembl
Outerchr11:14546001..14548200hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951312
Supporting Variants
SamplesBILGI_BIOE
Known GenesPSMA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998154
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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