A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077760



Internal ID18969403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46939697..47139213hg38UCSC Ensembl
chr1:47405369..47604885hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38199517
hg19199517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769552
SamplesKWP1
Known GenesCYP4A11, CYP4A22, CYP4X1, CYP4Z1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077760
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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