A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149659



Internal ID18852560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:7057617..7057691hg38UCSC Ensembl
Outerchr16:7107618..7107692hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000963
SamplesKWB1
Known GenesRBFOX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149659
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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