A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124632



Internal ID19256644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133772575..133787422hg38UCSC Ensembl
Outerchr10:135509900..135524800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3814848
hg1914901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv560n106
Supporting Variantsnssv3976687
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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