A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000922



Internal ID18844047
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 StatusS
Merged Variantsnsv1149619
Supporting Variants
SamplesKWB1
Known GenesLINC00494
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000922
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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