A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149619



Internal ID18855709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47895278..48516466hg38UCSC Ensembl
Outerchr20:46524022..47133004hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38621189
hg19608983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000922
SamplesKWB1
Known GenesLINC00494
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149619
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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