A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998366



Internal ID17291318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:70294584..70302083hg38UCSC Ensembl
Outerchr14:70761301..70768800hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952863
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998366
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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