A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125336



Internal ID18912568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76030224..76030322hg38UCSC Ensembl
Outerchr10:77789982..77790080hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983511
SamplesKWS2
Known GenesC10orf11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125336
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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