A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120883



Internal ID18933340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24811628..24817743hg38UCSC Ensembl
Outerchr6:24811856..24817971hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386116
hg196116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3290n106
Supporting Variantsnssv3963331
SamplesKWS2
Known GenesFAM65B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120883
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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