A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978966



Internal ID18897333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47895236..48516320hg38UCSC Ensembl
Outerchr20:46523980..47132858hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38621085
hg19608879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140253
Supporting Variants
SamplesKWS2
Known GenesLINC00494
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978966
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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