A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141941



Internal ID18922063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89124021..89124091hg38UCSC Ensembl
Outerchr16:89190429..89190499hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993446
SamplesKWS2
Known GenesACSF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141941
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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