A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954064



Internal ID17302938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:55801945..55809444hg38UCSC Ensembl
Outerchr20:54377001..54384500hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999999
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954064
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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