A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125353



Internal ID19276208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:78665873..78697464hg38UCSC Ensembl
Outerchr13:79240008..79271599hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3831592
hg1931592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960846, nssv3983528
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125353
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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