A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141978



Internal ID19267666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:147964294..147964373hg38UCSC Ensembl
Outerchr3:147682081..147682160hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993490
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141978
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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