A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003188



Internal ID16949454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:45906716..45907116hg38UCSC Ensembl
Outerchr20:44535355..44535755hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956210
Supporting Variants
SamplesBILGI_BIOE
Known GenesPLTP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003188
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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