A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125310



Internal ID19261285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40821909..41125267hg38UCSC Ensembl
Outerchr19:41327814..41631172hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38303359
hg19303359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983482
SamplesKWS2
Known GenesCYP2A13, CYP2A6, CYP2A7, CYP2B6, CYP2B7P, CYP2F1, CYP2G1P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125310
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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