A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110949



Internal ID19283013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:138617976..138618027hg38UCSC Ensembl
Outerchr3:138336818..138336869hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961371
SamplesKWS1
Known GenesFAIM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110949
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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