A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116452



Internal ID18902415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26891484..27356015hg38UCSC Ensembl
Outerchr10:27180413..27644944hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38464532
hg19464532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978633
SamplesKWS2
Known GenesACBD5, ANKRD26, LINC00202-1, LRRC37A6P, MASTL, YME1L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116452
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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