A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149126



Internal ID19199013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41693609..41713110hg38UCSC Ensembl
Outerchr10:42527099..42546600hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819502
hg1919502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002636
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149126
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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