A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067931



Internal ID18979589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187505468..189617277hg38UCSC Ensembl
chr4:188426622..190538431hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg382111810
hg192111810
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768440
SamplesKWP1
Known GenesLINC01060, LOC339975, TRIML1, TRIML2, ZFP42
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1067931
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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