A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110882



Internal ID19263387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:232368137..232368225hg38UCSC Ensembl
Outerchr1:232503883..232503971hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961294
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110882
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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