A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153497



Internal ID18848450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:24595881..24953312hg38UCSC Ensembl
Outerchr13:25170019..25527450hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38357432
hg19357432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001416
SamplesKWB1
Known GenesATP12A, CENPJ, RNF17, TPTE2P1, TPTE2P6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153497
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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