A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141985



Internal ID19283526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:26411825..26436995hg38UCSC Ensembl
Outerchr4:26413447..26438617hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3825171
hg1925171
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993496
SamplesKWS2
Known GenesRBPJ
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141985
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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