A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125281



Internal ID19286546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:67667343..67700171hg38UCSC Ensembl
Outerchr13:68241475..68274303hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3832829
hg1932829
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv988n106
Supporting Variantsnssv3983452
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125281
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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