A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954022



Internal ID16956209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:32445698..32482397hg38UCSC Ensembl
Outerchr20:31033501..31070200hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3836700
hg1936700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999962
SamplesBILGI_BIOE
Known GenesC20orf112
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954022
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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