A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078298



Internal ID18973935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4973913..4994163hg38UCSC Ensembl
chr10:5016105..5036355hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3820251
hg1920251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770820
SamplesKWP1
Known GenesAKR1C1, AKR1C2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078298
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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