A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999986



Internal ID17292938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47798357..47805056hg38UCSC Ensembl
Outerchr20:46427101..46433800hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954050
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999986
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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