A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998411



Internal ID16944677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101781364..101783663hg38UCSC Ensembl
Outerchr14:102247701..102250000hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952251
Supporting Variants
SamplesBILGI_BIOE
Known GenesPPP2R5C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998411
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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