A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073089



Internal ID18973075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64088635..64088915hg38UCSC Ensembl
chr20:62719988..62720268hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765952
SamplesKWP1
Known GenesOPRL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073089
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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