A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120098



Internal ID18937090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:92445323..92477049hg38UCSC Ensembl
Outerchr13:93097576..93129302hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3831727
hg1931727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960847
SamplesKWS1
Known GenesGPC5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120098
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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