A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073085



Internal ID18972855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63650146..63651047hg38UCSC Ensembl
chr20:62281499..62282400hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769979
SamplesKWP1
Known GenesSTMN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073085
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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