A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110896



Internal ID18913377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:109785618..109785791hg38UCSC Ensembl
Outerchr12:110223423..110223596hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961311
SamplesKWS1
Known GenesTRPV4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110896
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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