A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955149



Internal ID16957336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62201145..62230644hg38UCSC Ensembl
Outerchr20:60776201..60805700hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3829500
hg1929500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000011
SamplesBILGI_BIOE
Known GenesHRH3, MTG2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955149
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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