A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150609



Internal ID19197123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170141229..170265211hg38UCSC Ensembl
Outerchr6:170456453..170574299hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38123983
hg19117847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996090
SamplesKWB1
Known GenesLOC154449
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150609
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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