A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150745



Internal ID19200140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:4332807..4334808hg38UCSC Ensembl
Outerchr10:4374999..4377000hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996218
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150745
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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