A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148754



Internal ID19198401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125887930..125925531hg38UCSC Ensembl
Outerchr10:127576499..127614100hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3837602
hg1937602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997542
SamplesKWB1
Known GenesFANK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148754
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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