A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153447



Internal ID19201980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49254525..49254582hg38UCSC Ensembl
Outerchr10:50462570..50462627hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001364
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153447
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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