A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140340



Internal ID18931808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:275420..275504hg38UCSC Ensembl
Outerchr3:317103..317187hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979049
SamplesKWS2
Known GenesCHL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140340
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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