A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151292



Internal ID19195655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41842909..41885273hg38UCSC Ensembl
Outerchr10:42354899..42397300hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3842365
hg1942402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003858
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151292
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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