A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116508



Internal ID19259574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:91609032..91627329hg38UCSC Ensembl
Outerchr13:92261286..92279583hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3818298
hg1918298
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978693
SamplesKWS2
Known GenesGPC5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116508
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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