A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125350



Internal ID19270587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21949710..21956223hg38UCSC Ensembl
Outerchr13:22523849..22530362hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg386514
hg196514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983525
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125350
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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