A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983452



Internal ID19233925
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 StatusS
Merged Variantsnsv1125281
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983452
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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