A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125299



Internal ID19267525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41710705..41840838hg38UCSC Ensembl
Outerchr10:42399371..42529504hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38130134
hg19130134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983471
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125299
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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