A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979059



Internal ID18894144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:82492351..82492415hg38UCSC Ensembl
Outerchr4:83413504..83413568hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140350
Supporting Variants
SamplesKWS2
Known GenesTMEM150C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979059
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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