A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150330



Internal ID19200850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:152972272..152972353hg38UCSC Ensembl
Outerchr6:153293407..153293488hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003631
SamplesKWB1
Known GenesFBXO5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150330
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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