A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118487



Internal ID19280159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133774775..133787422hg38UCSC Ensembl
Outerchr10:135512100..135524800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3812648
hg1912701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv560n106
Supporting Variantsnssv3958996
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118487
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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