A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110838



Internal ID19275054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:172455534..172456273hg38UCSC Ensembl
Outerchr3:172173324..172174063hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2637n106
Supporting Variantsnssv3961247
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110838
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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