A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078896



Internal ID19324605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10027827..10033794hg38UCSC Ensembl
chr3:10069511..10075478hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg385968
hg195968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771521
SamplesKWP1
Known GenesFANCD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078896
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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