A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124939



Internal ID18930537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:57340802..57420102hg38UCSC Ensembl
Outerchr6:57205600..57284900hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3879301
hg1979301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3320n106
Supporting Variantsnssv3977745
SamplesKWS2
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124939
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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